Tag | Content |
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EnhancerAtlas ID | HS054-00077 |
Organism | Homo sapiens |
Tissue/cell | FT246 |
Coordinate | chr1:16507080-16509430 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ELF3 | MA0640.1 | chr1:16508229-16508242 | CTACTTCCGGCTA | - | 6.25 | EWSR1-FLI1 | MA0149.1 | chr1:16508479-16508497 | GGGAGGAAGGAAGCAGAG | + | 6.42 | LMX1B | MA0703.2 | chr1:16507192-16507203 | ATTTTAATTAA | + | 6.62 | Lhx3 | MA0135.1 | chr1:16507206-16507219 | AAATTAATTATTT | + | 6.78 |
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| Number of super-enhancer constituents: 28 | 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_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 | chr1:16507488-16507895 | Ovary | SE_47009 | chr1:16508039-16509386 | Ovary | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16507579-16507933 | Pancreas | 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: 2 | Chromosome | Start | End |
chr1 | 16508086 | 16509162 | chr1 | 16508402 | 16508642 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | GAATGATGAA TGGATAGAAA CGTTTTACAT CTGCTCCGCA CTGGCCGCAC GCGGCTACTG 60 AGCACTTGAG ATGCGTCTGG TGCACCTGAA GAGCTGACTT TAATTTTATT TCATTTTAAT 120 TAATTTAAAT TAATTATTTG TTTATTTGAG ACAGAGTCTC GCTCTGTCAC TCAGGCTGGA 180 GTACGGTGGC GCAATCACAG CTCACTGCAA CCTCTGCCTT CTGGGCTCAA GCCAGCCTCC 240 TACCTCAGCC TCCTGAGTAG CCAGGACTAC AGGTGTACAC CACCACACCC AGCTAATTTT 300 TTGCGTGCTT TTTGTAGAGA TGGGGTTTCA CCATGTTGCC TAGTCTGGTC TCGAACTCCT 360 GACCTCAAGA GATCCACCCA CCTTGGATCC CAAAATGCTG GGATTACAGG CATGAGCTAC 420 TGCGCCCGGC CTCTAGATTT AAATAGTACC TACCGAACTG GCCAGTGCAG CTCTAAAAGG 480 TCAGCAGCAT GTGAGTGGGA GAGCTGGGCC TGGCTGTGTG TTATTCACGT TCTTGAGTGT 540 TGGCTTTCCA CAGTTTGGGC CTCTGGCAGC AGAATCACCT GGGAAGCCAA AACTTCAGAT 600 CCCTGGGATC CCAGACCCAC TGAATCAGAA TCTCCGAGGC CAGGGCTTGG GCGTCTGCCC 660 GTTCACCACA CACCCCAGCT GATTCTGATG CACATGAGGT CAAGTTTGAA ACCCACCCCA 720 CTGCCCTAGT TGTTCAAGAC TCCCAGCGCT GGCTGGATGC AAAGTCTTAT GCCTGTAATC 780 CCAGCTCTTT TGGGAGGCCA AGGCGGGCAG ATCACTTGAG GTCAGGAGTT CGAGACCAGC 840 CGGGCCTACA GAGTGAAACC CCGTCTCTAC TAAAAATACA AAAATTAGCT AGGTGTGGTG 900 GTGGGCGCCT GTAATCCCAG GAGGTGGAGG TTGCAGTGAG CCGAGATCGC GCCGCTGCAC 960 TGCATCCTGG GCAACAGAGC GGGACTCCGT CTCAAAAAAA AAAAAAGACT CCCGGCCAGG 1020 AAGAGAGCTT GAATGAAGTC TGACCTGCAC CAGGCCTTCT GGGCCCAGAC CAGGCCTGCT 1080 TAGGGGCATG TGCCCTGCTC AGAACTTCCC CATCCCAGCT AACCCAGAAG ATAGCTGGGA 1140 TGAAGATAGC TACTTCCGGC TACCAGCCCA TGATTCTTTG CCAGCCTGCA CTGTTCCCTG 1200 AAGAGCAAAA AGACTTGGAA TTTCCCTGCT CTATCCAGAG GGGCTGGGAT GAGGGGTCCT 1260 GAGTTCCCTT ATCCCATGTC CTACCAACCT CTGGAGCTCT CCAGTCAGCC AGCTCGAGGC 1320 TCTGGCCCTA GCTGGTGGGC AATGGGAGGG AGAGGCTTGG CCCAGCACCC CACCCCACAG 1380 ATCAGCCTGG TCCGGCAAGG GGAGGAAGGA AGCAGAGGCA GCCTGGGCCA GCGGACACAG 1440 GGTTGGGGGT GACACAGGCC TCAGGAATTT GAAAACAAAC ACTTCGCCAG GGAAGGAAGA 1500 GGCTGCTGTT GGCTGCTGAG CCCGGGCGGG CCCAGGTCCC TCCCTTTCAG GGCAGGGGTG 1560 AATCCCAGTG CTGCTGACCA TGGCCCCCGG CTGGACCCAG TGCTCGGGGA GTTTCCACTC 1620 CGCTGGTGGG ATGGGAAGGT CATGGGAGGT GTGGGGGGAT CCAGGCTCTG TCCAGATACG 1680 GGAGCATCCT GGCTGGGGTG AGGACAGGAA GGGACAAAGA GCTGGGAAAG CCACGAGACC 1740 CCAGGAGAAG GCTCAGCAGC AACAGGATGC CGCCTCAAGC ATTTATTGAG CACCCATGGT 1800 ATTCCAAAAA CTGAGAATAT AAGCACTGCC TAGCTGGGGA GATCAGGGGA AGCCTAGAGC 1860 CCTGTGGCCT TCCTGGAGGA GGTGGCATTG AACTGAGCCC TGAAAGGTAA ACTAGGACCG 1920 GGGAGGACAG AATCTTACAA GTCTCCCCCC TTCACACTCC CAGAGCCGGC GCTCAGTGAG 1980 TGCATGAGTG AGTAAGCGGC TGACCAGCGA CTATGCAGCA TGAATGAATG ACAGACTGAA 2040 TGACATGAAG CCTGGAGTCT CAAGGCCGAG ACTGCAAAAG AAGAGTCCAT CCTCCTATCC 2100 CCTCTGCTCT GAACTCTCTT CATGATCCTG AAGGTGCTTG GTACCTGGAG ACTACGGAGC 2160 CAGCCTGCCG GGGTTCTAGT CTGAACTCAG TCACTTCCCA GCTGTGTAAC TTTGGACAAG 2220 TTACTTAACC TCTCTGTGCC TCTGGTCCCT TCTCTGTAAA GTGTAGTCAT CGGCCGGGCG 2280 TGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCAGACGA ATCACTTGAG 2340 GTCAGGAGTT 2350
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