Tag | Content |
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EnhancerAtlas ID | HS050-21915 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr14:104159180-104160600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:104160575-104160596 | CGTGTGTTTCACTTTTTTTTT | + | 6.53 | SP3 | MA0746.2 | chr14:104160006-104160019 | TGCCACGCCCCTC | + | 6.08 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_24470 | chr14:104159192-104160636 | Colon_Crypt_2 | SE_26911 | chr14:104159062-104160781 | Esophagus | SE_32310 | chr14:104159095-104160464 | Gastric | SE_41604 | chr14:104159140-104159852 | LNCaP | SE_41604 | chr14:104159891-104160510 | LNCaP | SE_60612 | chr14:104145010-104184512 | DHL6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I103690 | chr14 | 104157271 | 104161386 |
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Enhancer Sequence | GTTAACATGA TGACTAGCGT GCTGTCAGTT TGACACTAAA ACCTGAAGCA CTCGGTGCAG 60 TTGCTCGGGC CTCACACAGA CACATCAGGT TTACATCTGA AAGTACTGCC TCCCTTCCCC 120 ATCACGGAGG CCGTTTGAGT TTTCATCCAC TCCGCCCTTT GGTGTGGCTG TCAGTGGGTG 180 GCCGGGTGCC TGTGGCTGCT CTAGAACCTG TTTCTCAGGT GCCTGGGGCC CACCCGGCAG 240 CTCGAGCTGT TGGGACTTGG CAGTCCCTGC CCCTGTGCTG GTGCTGAGAG TTCGCGACAG 300 TGGCCAGGCA CTGCCCTCCC AGTTGTCCAG ATCCACTAAT CCTCACAGAC AGGCCAGTGC 360 CCCGACCTGT CCCCCAACAC TCTTGGGAGG CAGCCATCTC GGGAAAGCTT TTCCCCAGCC 420 CCCTTCTCGG TGGCTGTTAA AGAGGCTTGT AGGGTGCTGG ACATGTTGCT TGAAGCACCC 480 CTAATGACAA GAGGAAAGAA AGTCTCTTCA TTTTACAGGG TCCTGTAGCT GACCCAGTGT 540 TTGCCCTCCA GTTTCTTGGA GTTTCTACAT GCACATTGAC CCCTGGGCCT CTCGAGTGCC 600 AACCTAGATT TAGCTGTGCA GCTGGTACTG TTAGGCCTGA GGCCATTTGA AGCTGGCATC 660 ATTTGAAGTC CTGGTTAAGT GTAATTTTTC TATTTGTTTT TTCATGCAGG AACGAAATAA 720 TTGTCTGGCC GACTCGCGAG CTCTGAGTGC CAGCCACACT GACCTGGCCC ACTGAGAGCC 780 AGCAGGGCTA GGTAACCTGT CTTGGGAGTG TGAGACCGCC CCGCCCTGCC ACGCCCCTCA 840 CCGCCCTGCC CGGAGGCGCC AGCCGCACTC CTTGGCTTCC TTTCCTAGAT AGTGACGTCC 900 ACCAACCTTG GAGGTGCCTT TTCAAAACAC CCGGGAGGCC GTGCCTCAGC ATTCTGTTAC 960 TCGGCCTGCA GCCCCAGTGC CAGGAGCCAC CCCGACCGCG ACCCGGCCAG GCTGGCTCAG 1020 GGAGGCCGAG GTGGCGCTGA GGTGGCTTCA GCACGCTGGG GATTGGCTCC TGCTCACGGA 1080 TGCTGTTGCA TTTCCTGCCT GCCACCTTTT TGCCATGACA CCAGACTCTC TTTTAAATTG 1140 TAATATTGTA ATAAGGCTGT AAATTAAGAA TCTGGAAACA TAAAGTACCC CTTTCAGAAC 1200 GATAGGCATT TAGTGATCTA TGGCAGTAAA GCCTGAAGCT TAGCGGACAC TGGTCAGTGG 1260 GAAGTGAATT CCTTCCCAGC TGGAGCATCT TCCGGGTCTC TCTTTCCAAG GTCCCCATGC 1320 CTGTGGCCCT GGGGCCCCAT GCCCCCTTTT GAGCTGTGTT CTCCCGGACG CCCCTGCACA 1380 CGAAGCCCAT AGAGACGTGT GTTTCACTTT TTTTTTTTTT 1420
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