Tag | Content |
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EnhancerAtlas ID | HS104-00557 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr1:16498650-16500970 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | - | 7.07 | MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | + | 7 | RREB1 | MA0073.1 | chr1:16498769-16498789 | CCCCCTCCCACCCCACCCCA | + | 6.5 | Spz1 | MA0111.1 | chr1:16499568-16499579 | AGGGTATCAGC | + | 6.32 | ZEB1 | MA0103.3 | chr1:16500289-16500300 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16497584-16499266 | Colon_Crypt_1 | SE_23091 | chr1:16499347-16501823 | Colon_Crypt_1 | SE_23751 | chr1:16497995-16499231 | Colon_Crypt_2 | SE_23751 | chr1:16499364-16501671 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_26540 | chr1:16496436-16504779 | Esophagus | SE_28102 | chr1:16497879-16504574 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16497806-16499321 | Gastric | SE_31527 | chr1:16499336-16504399 | Gastric | SE_34268 | chr1:16497740-16504248 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_36144 | chr1:16498765-16501519 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_44998 | chr1:16499693-16500212 | NHLF | SE_46140 | chr1:16499323-16500582 | Osteoblasts | SE_47150 | chr1:16497663-16499232 | Panc1 | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16499523-16500148 | Pancreas | SE_47539 | chr1:16500355-16501118 | Pancreas | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16497970-16501408 | Small_Intestine | SE_56795 | chr1:16496450-16499306 | VACO_400 | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16499350-16500174 | VACO_503 | SE_57357 | chr1:16500236-16501136 | VACO_503 | SE_57939 | chr1:16499369-16500862 | VACO_9m | SE_64726 | chr1:16499137-16501292 | NHEK | SE_65472 | chr1:16498579-16501949 | 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 | 16499607 | 16500371 | chr1 | 16499761 | 16499895 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | TCTCCCCCAC TGTAAACCTG CAAGGGCAGC CACGGCCGGG AGCAGCTGGT CCTGAGACTT 60 GGGCAGAGGC CCTGGACAGT GGGGCAGAAG CGCTTGGCTG GCCAGGAATT GGATCACTGC 120 CCCCTCCCAC CCCACCCCAT TCAGCCCTGT CTCCCACGGA CTCTGACCAC CCCTTGGTTC 180 TCTTATCAAA AACCGCCAAA ACCCGCCATC GAAACTCCCA GCCTCCTGAC CCCCATGCCC 240 CACCCGGCTC CACCCGTCTT CCCAACCTGG CATCCAGTGC CCCAAACCTG CCTATTCCGT 300 TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT GGCACCAGGA GGCCAACAAC CCAGGCCCCC 360 TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC CTCCACCCTA CTGTTTCTCC TGGGGTGTGC 420 CTTTCTTTGC CTTATGCCTC GGCATCTCTA AGTGGCAGGG GATGGAGTGG AGTGAGGGCG 480 GCAGGCCAAG GGCATGGCCC ATAATGAAAA AGGAATCTGG TTGGGCATGG TGGCTCACCC 540 TTGTAATCTC AGCACTTTGG GAGGCCAAGG CAGGCAGATC ATGAGGTCAG GAGATCGAGA 600 GCAGCCTAGC CAACATGGTG AAACCCCGTC TCTACTAAAA ACACAAAAAT TAGCTGGACG 660 TGGTGGTGGG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATTGCTGGAA 720 CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG ATCACGCCAT TGCACTCCAG CTGGGGCCAA 780 CAACAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AGAAAAAGGA ATCTGAGCAT 840 GGAGGCACCC TCCACCTTCG GATTGCTAGG AGATCAATGT CTGGCCCCGA GTGGGTGAGG 900 CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA GTTCACGGGG CCTCTTCCTC 960 TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG CAGGAGTCCA GGCTCATAGA 1020 GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA CCATTCCCAC TGGGGCATAC 1080 AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT TTTGCGGAAG AACTAACCAC 1140 ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG TGAGTCAGTT TTATTATATG 1200 AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC ACACAGACAG TGCTCAGCGA 1260 AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT CCCCAGCTTC TCTGGGGGAT 1320 CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC ACTACTCCCA GCCTTTGTCC 1380 CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT GGAGCTTCCT CCTCTGGTCC 1440 TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG 1500 CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG CCCAGGCCTC GGGCAAACAG 1560 AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG 1620 CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG ACACCTGCCT CTGTTACCTT 1680 GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC CTGGGGCAGG GGGATGGAGT 1740 GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT TGAACAAGGC CTCTCTGAGC 1800 CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT AGCCTTCTGG TGGGCTTATG 1860 GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA TCAGCCTGCC TCACCGTGAG 1920 GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG GGGGTCTTCT GGCTCTGGGC 1980 CCTAGAATGG GGCTGAAGCC CAGAGAGGCA GTTGCACCTC CCCTAGGCCA CACAGCAGGT 2040 ATAGGCCCCA GGGGCTGAGT GCCCATCATG CCTGCCCTCC TCTCCATCCA CCCAGAGCCT 2100 CACTAGCCAG ACCCGCACTC TCCCATCCCC TGGGCAAGTC TGCACCCCAG GTCGGTGAGG 2160 ACTCCCAGAT TCTACTCCCA CCAGCCAGGG CCAGACCTGG TGCAGGAGGC TCCACAGTTC 2220 TCCTGCTCGG GGCTCCGTCT CCCCACTTCC TGGAGCTCCA TCCAAGTGGG GAACCCTGCC 2280 CGTCCTCTGC CCCTCAAGCC AACCAGGCAT TTACGGGGGA 2320
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