Tag | Content |
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EnhancerAtlas ID | HS053-00428 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:16507550-16511900 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Arntl | MA0603.1 | chr1:16510043-16510053 | GGTCACGTGC | + | 6.02 | ELF3 | MA0640.1 | chr1:16508229-16508242 | CTACTTCCGGCTA | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr1:16508479-16508497 | GGGAGGAAGGAAGCAGAG | + | 6.42 | IRF1 | MA0050.2 | chr1:16511877-16511898 | TTTTTCTTTTTTTTTCTTTTT | + | 6.07 | Nr2f6(var.2) | MA0728.1 | chr1:16509417-16509432 | GAGGTCAGGAGTTCA | + | 6.22 | STAT1 | MA0137.3 | chr1:16511012-16511023 | TTTCCTGGAAA | - | 6.62 | Stat4 | MA0518.1 | chr1:16511009-16511023 | CCTTTTCCTGGAAA | - | 6.91 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16507977-16509332 | Colon_Crypt_1 | SE_24743 | chr1:16508183-16508861 | Colon_Crypt_3 | SE_26540 | chr1:16504790-16512175 | Esophagus | SE_28102 | chr1:16507825-16509373 | Fetal_Intestine | SE_29455 | chr1:16507734-16509371 | Fetal_Intestine_Large | SE_31527 | chr1:16507486-16509710 | Gastric | SE_31527 | chr1:16509851-16511737 | Gastric | SE_34268 | chr1:16506936-16512113 | HCT-116 | SE_34628 | chr1:16506549-16512234 | HeLa | SE_36144 | chr1:16507720-16509431 | HMEC | SE_38062 | chr1:16507125-16509874 | HUVEC | SE_40833 | chr1:16507342-16509479 | Left_Ventricle | SE_44998 | chr1:16507356-16509449 | NHLF | SE_46140 | chr1:16507347-16510631 | Osteoblasts | SE_47009 | chr1:16508039-16509386 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16507961-16508560 | Pancreas | SE_47539 | chr1:16508587-16509159 | Pancreas | SE_48744 | chr1:16507441-16509527 | Right_Atrium | SE_50427 | chr1:16507395-16509522 | Sigmoid_Colon | SE_52536 | chr1:16507445-16509419 | Small_Intestine | SE_56795 | chr1:16507333-16512008 | VACO_400 | SE_57357 | chr1:16508000-16508578 | VACO_503 | SE_57357 | chr1:16508592-16509318 | VACO_503 | SE_57939 | chr1:16507977-16509011 | VACO_9m | SE_64726 | chr1:16507942-16511421 | NHEK | SE_65472 | chr1:16507356-16509554 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr1 | 16508086 | 16509162 | chr1 | 16509950 | 16510149 | chr1 | 16508402 | 16508642 | chr1 | 16510864 | 16511423 | chr1 | 16511499 | 16511858 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | CTCTAAAAGG TCAGCAGCAT GTGAGTGGGA GAGCTGGGCC TGGCTGTGTG TTATTCACGT 60 TCTTGAGTGT TGGCTTTCCA CAGTTTGGGC CTCTGGCAGC AGAATCACCT GGGAAGCCAA 120 AACTTCAGAT CCCTGGGATC CCAGACCCAC TGAATCAGAA TCTCCGAGGC CAGGGCTTGG 180 GCGTCTGCCC GTTCACCACA CACCCCAGCT GATTCTGATG CACATGAGGT CAAGTTTGAA 240 ACCCACCCCA CTGCCCTAGT TGTTCAAGAC TCCCAGCGCT GGCTGGATGC AAAGTCTTAT 300 GCCTGTAATC CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG ATCACTTGAG GTCAGGAGTT 360 CGAGACCAGC CGGGCCTACA GAGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCT 420 AGGTGTGGTG GTGGGCGCCT GTAATCCCAG GAGGTGGAGG TTGCAGTGAG CCGAGATCGC 480 GCCGCTGCAC TGCATCCTGG GCAACAGAGC GGGACTCCGT CTCAAAAAAA AAAAAAGACT 540 CCCGGCCAGG AAGAGAGCTT GAATGAAGTC TGACCTGCAC CAGGCCTTCT GGGCCCAGAC 600 CAGGCCTGCT TAGGGGCATG TGCCCTGCTC AGAACTTCCC CATCCCAGCT AACCCAGAAG 660 ATAGCTGGGA TGAAGATAGC TACTTCCGGC TACCAGCCCA TGATTCTTTG CCAGCCTGCA 720 CTGTTCCCTG AAGAGCAAAA AGACTTGGAA TTTCCCTGCT CTATCCAGAG GGGCTGGGAT 780 GAGGGGTCCT GAGTTCCCTT ATCCCATGTC CTACCAACCT CTGGAGCTCT CCAGTCAGCC 840 AGCTCGAGGC TCTGGCCCTA GCTGGTGGGC AATGGGAGGG AGAGGCTTGG CCCAGCACCC 900 CACCCCACAG ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA AGCAGAGGCA GCCTGGGCCA 960 GCGGACACAG GGTTGGGGGT GACACAGGCC TCAGGAATTT GAAAACAAAC ACTTCGCCAG 1020 GGAAGGAAGA GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG CCCAGGTCCC TCCCTTTCAG 1080 GGCAGGGGTG AATCCCAGTG CTGCTGACCA TGGCCCCCGG CTGGACCCAG TGCTCGGGGA 1140 GTTTCCACTC CGCTGGTGGG ATGGGAAGGT CATGGGAGGT GTGGGGGGAT CCAGGCTCTG 1200 TCCAGATACG GGAGCATCCT GGCTGGGGTG AGGACAGGAA GGGACAAAGA GCTGGGAAAG 1260 CCACGAGACC CCAGGAGAAG GCTCAGCAGC AACAGGATGC CGCCTCAAGC ATTTATTGAG 1320 CACCCATGGT ATTCCAAAAA CTGAGAATAT AAGCACTGCC TAGCTGGGGA GATCAGGGGA 1380 AGCCTAGAGC CCTGTGGCCT TCCTGGAGGA GGTGGCATTG AACTGAGCCC TGAAAGGTAA 1440 ACTAGGACCG GGGAGGACAG AATCTTACAA GTCTCCCCCC TTCACACTCC CAGAGCCGGC 1500 GCTCAGTGAG TGCATGAGTG AGTAAGCGGC TGACCAGCGA CTATGCAGCA TGAATGAATG 1560 ACAGACTGAA TGACATGAAG CCTGGAGTCT CAAGGCCGAG ACTGCAAAAG AAGAGTCCAT 1620 CCTCCTATCC CCTCTGCTCT GAACTCTCTT CATGATCCTG AAGGTGCTTG GTACCTGGAG 1680 ACTACGGAGC CAGCCTGCCG GGGTTCTAGT CTGAACTCAG TCACTTCCCA GCTGTGTAAC 1740 TTTGGACAAG TTACTTAACC TCTCTGTGCC TCTGGTCCCT TCTCTGTAAA GTGTAGTCAT 1800 CGGCCGGGCG TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCAGACGA 1860 ATCACTTGAG GTCAGGAGTT CAAGACCAGC CTGCCCAACA TGGTGAAACC CTGTCTCTAC 1920 TAAAAACACA AAAATCAGCC GGGTGTCGGG GGCAGGCACC TGTAATCCCA GCTACTCGGG 1980 AGGCTAAGGC ACGAGAATTG CTTGAACCCG GGAGGCGGAG GTTGCAGTGA GCTGACATCT 2040 CGCCACTGCA CTCCAGCCTG GGCAACAGAG TGAGACTCAA AAAAAAAAAA AAAAAATACA 2100 GAGGTAATCA TAGTGCCTCC TTCACAGGGT TTTTGAGAGG ACTGAATGAG TTTTACAAGT 2160 GAAGTGCTTA GAACGACGTT GCACATGTAG TGAGAACTAC ATGAGTGTTG GCCAATGCTA 2220 TTACTGAGGT TCCAGCTTAC GCGTTCATTG AGTCACTCAC TCACTCACTG TTCATTCACT 2280 GATTCGCTCC TACATGCCAT CCGCCACTTA CACACCCCTC CCTCTTCACC GTCATCTGTT 2340 AAGCAATCCC CGTGTGCCCG GCTCTCTCCT CTCGGTCCTC CCAGCCCCCC TTTGCCAGTC 2400 TTGGATGGTG CCCGCCGTGC TGCCAATTAC CCTAACAATT TCATTAATTC CTCTCAAGCC 2460 CAAAACAAAC AAGAAGGACC TATCTGGAGC AGGGGTCACG TGCTAAGACC AGAAGCAGGT 2520 GTGGGACAAA CCCTCTAGGA CGAGTTCTTT GACCAGAGTT CATCACCGGA GCTGCTCCAG 2580 AGATGGCCAG GCCTCCCCAC CTGCAGGTGC CCGGCCAGTG CCCCCCACCC CGGGCAGCCT 2640 CACCCACTCC CCTCTTTGAG TAAAGGTAAA GGGACTTGCC CAAGGCTGGG TTCTCCCACA 2700 TCCCGACTGC ACCTGTCCAC ATTTCAGGCT TCATTCATGC CAGGAGCCCC AGACCTGCTC 2760 CATGCACCAG CTCCGCCCAA GCCTGGAGCC CCGGGCTGGC TGAGGTGAGA GCCCCAAAGC 2820 TCGAGCCCAT TTCAGCAGCT AACAATTAGA GCTGGTGTGA ACATGATGAC TGCATGCTGA 2880 TTAATGTAAG ATGGCTGAGC AGAAGATCCC GCCATTTCCT TCCCCACAGG CCCTGGGAGA 2940 ACAGGTCCCG CTGGGGAAGA CTCTGTCGTG TTCTGCAAAA GCCATTTCTT GAGCACGTCC 3000 TGCAGGCCGG GCACTGCGCT GGGCACTTGA TTCCTTTCAA CAGCATGACA TGGTGGGAGG 3060 ACAACTTGCC TCTCATTGAT GAAGAAACGG AGGCTCAGAG AGGTAAAGGA ACTTGCCCAA 3120 GGCCACACAG CCAGTCAGTG TGGTCCTGGA ATTCCAATCC AGGTCTTCTC TTGCTGATTC 3180 CTACCCCCAG GGATGAGCCA GTTTGACATT TGTGGAACTG GAGAGAGGCT GGGTTTGGGC 3240 ATAAGGTAAT GTTTAGGCCA GAGGGTGGAG AAGGAGAGGA CAGCCAGAGA GGCAGAGCCA 3300 AGCGCCAGGC AGGAACAATG GTACAGGGCA GGTAACGGGA GCCCGGCCAG CTCTGGGACT 3360 CCTGGGCAGG CCCTGCTGGG CCCTGCGAGC AACAGGCTCA CCCTGTGGAG CTGCCAGGGT 3420 GACAGCAGCC TCGATCTGCT GACTCAACGA GTGCATCGGC CTTTTCCTGG AAAACAGTAG 3480 ACGCAGTGTG GGTGTCGGAG GGAGGCACCT GTTTGGGAAA AGGGTGTGTG GGAACCCTGT 3540 CCTGCCCTGC AGCTCCCCAC AGCCAGTGTA CAGGTACTTA GCTCCAGGTG CCCCCCGAAC 3600 CTCCCACCAC CTGCCCAGAC CCCAGAAGCC ACCGGATCCA GGAGTCCGAG CCAGCTGTGG 3660 GCTGAGTCCA TGGTGCCACC AAGGCTCTGC ATGACCAGTG CTGCCAGCCA CCACCTCAGC 3720 CAAGCAGCAC AGCCTCTCAG GGCATGTCCC CACTTGCTGT CTGCAGAGCC TTGTTTTGCC 3780 CCACCCTGAA GGGGCAGGTG TAGACGAGCA TTGAGGCAGG TCTATGTGAC ACCACTTGCT 3840 GTCACTCTTC TTTGGGAGGT ATCAGGGCCA CTCTGCCACG GGGCACAGCT TAGGGCCTCC 3900 ATGGAATCTG GTCTGAAGGA TCCCGCTGCC CAGAGGGGGG TCAAGAATAC GGAATGGGTT 3960 CAGGAGCACC CCCTGTCTTC AGGATCCAGT TGGGGGAGGT CCCAGCAGGG CCAGTCACAG 4020 ACACTTGTCA CACCCTGGAG GGGATAATAG GATCTGGGGC TCAGCCTCCA CCAATTTCAT 4080 CACCACACAC CACACCCAGG CAAGGGAGAG CAGAGGCATC AGCAGGGCCT GGCTGAGGGG 4140 CTGAAGCCTG GTGGGGAAGC AGGGAGGGCC CCTGGGCCTC TCGGTCCTAT CTCTTCCCAA 4200 TCCAGGCCTC AGCGGACTCC AGGGCAGGGG TGCGGGAGCT GATTTCCAGG TGCAATATTC 4260 ACTGTCACCA TGGCCGCTTC CAGCACCCAG CCTGAATTTC CTAGTGCAAT GCTGGGAAGA 4320 ACTAGTCTTT TTCTTTTTTT TTCTTTTTTT 4350
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