Tag | Content |
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EnhancerAtlas ID | HS095-23155 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr4:148282840-148285120 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXC1 | MA0032.2 | chr4:148284389-148284400 | TATGTAAATAT | + | 6.62 | IRF1 | MA0050.2 | chr4:148284825-148284846 | TTTTGCTTTTAGTTTCATTAT | + | 6.95 | NR2C2 | MA0504.1 | chr4:148282971-148282986 | TGAGGGCAGAGGGCA | + | 6.14 | RREB1 | MA0073.1 | chr4:148284713-148284733 | CCACACCCCACCAACCCTCA | + | 6.26 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 148282893 | 148283000 | chr4 | 148283000 | 148283382 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I147359 | chr4 | 148280497 | 148285022 |
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Enhancer Sequence | GGAGATCTGA CCTAATTTCT CTTTAGGCCT ATTAGAAAAT GACATCCTTC CATTGGCAGA 60 AACTGTCTAA TTACTTTTTG TTATGAGCTA TTTCCAACAT TGCTGATCTG CAATTCTACA 120 GAGCACTTTC ATGAGGGCAG AGGGCAACTG TGAGTCATAG AGACTCTGGG AGGAAAGCAG 180 AGCTCTTTGT CTGAATAAGG AAAAGTTCAG TTGTTCCTTA GGTTTCGGGC ATATCAGCTA 240 TTGCTGTCAT TGGGAGTGTT TCCCAGAACT GAAAGTGAGC CTTTTAGAAA GGTTTGACAT 300 CAGGCAAGTG CTCTCTGGGG CAGGAGAGCT GCACTTTTCA GTGATAAGTA CAAAGCCTAG 360 GTTCCCTGAT GAATAACAGC TTGATGATAC TGGGTTAAGT TACTGAACTT CTCTATGAAA 420 TTACATCAGC CATACCATTA GGTTGTTTGG ACCATTCAAT GAAGTAAATA CATAAATGTA 480 CATAGCCCAT CACCTGCATA GATTATATCT TCCATAAGGA ATAGTTGCCT TCCTTCCTCT 540 TGGCTAAGGG AATTGGAGGT CTGGCTATAC TGTTGGAGAG AAGAGTTGTA CCACAAACAG 600 ACTCCACTGA AACCATGTGG ACTTTGGGAA GACTGGGCCC AAACCATAGC TCAGAAAGAA 660 CATTTGGTGA AGGAGCCCAG GTCTATCCAA CATGACAGCC ACTCTTCTTC ATGGTCTAGC 720 CTAGTGCTAT TCAAAGTGTG GTCCTTGGCC CAACTGTATC GATATCATCT CAGACCCTCT 780 AAATCTGGAT CTCTGGAGTA GGGCCCAAGA ATCTGTGGTT CTACCAGCTC ACCAGGTGAT 840 TCTTTTGCAG GCTCAAGTTT GAAAAACACT GCTTTAGAGA AAGTGTTCCT AGCAAACCCA 900 AGAGGACAGG AAGACATGGA CCAGGGTAAC AATCAGATTT TCAGGGGCTC AAGCCAAGGA 960 GGTTTTAAGA AAAGGTGTAA CAAATGACTG CTAGGAAGCC TCTGGGAAAA ACCTTTAGGA 1020 ATCATGTAAC AATTGTCAAT TTTATAAACA CTTTCGTTCA CTTAGCAAAC ATGAATCCAC 1080 ATGCGCTTAT TAATCTTCTA ACCAGAAGTA AGCCACTGAG TTTTTCACAA ATTGGCTGGA 1140 CAGGCTGATT CCCAAGACAA GAAGAGATCA TCCACAAAAT CCTTAAATAA AAAGAGCCTA 1200 AGTGCTCATT TTTGGTGACA GCAAGCAAAG AGGGAGATGG GAAGACAGCA TTTTACTCAG 1260 TAGTCAGTCG TAGGAGGAAA AGAACCAGGG AATGGAAGCA GTCCAAATCC CTAAGGCTTT 1320 CAGAAAGCAG GGGGAAAAAA TAAAAGCTAG ACATGGGACT GAAATCCAGA GGTTGAGACA 1380 TGACCCATCA GGCACATAAC TGGCAGGAAG CCCAGCAGCG AGGCTCCCTC TTAGGAACTA 1440 AGCATCTGCC TGTTTTCACG TCTCTGCAAC ATACTAAATT ATCTGTTAGC AAGTAGTTGC 1500 AGCATCCACA AAGATCAGGG ACACAGGACA CTTAGAAAAT TCAATTGTGT ATGTAAATAT 1560 TTACCTAGCT ACTTCCTTGG AGTCTACAGA CCTGTGACAT TTTATTGGCA GACAGACTTT 1620 ATGATTTCAG CGTGCCAGTG TATTTTATCA GAAATAAGTG AAAAAAAAAC TCAAAACAAC 1680 TTGGAAAATA GAGATGTTCA AGTCAAGGTT TATCCACCAA TGCCTCTGAA ACTGGAGGGG 1740 CTTCAGTGCA GACCTTTAAT CCACAATGCC TGATTCTGAA GTGGCATGTC TGTGTAAGAG 1800 AATTTAACAT CCTAAGGATC CGCCAGCCTC TTCTATTTAA AGTCAGGGCC ATTGATCCCC 1860 TTTTTGGGTT GACCCACACC CCACCAACCC TCAGGATCTG GATGCCATAT AAACATTAAC 1920 CAGAAGAAAT CAGTTGCGTA TCTCAGGTAG ATTTATCTTC TAGGTAATCT TATTCCTAGA 1980 CATGCTTTTG CTTTTAGTTT CATTATATTT ACTTTGCCTT TGCCCTGCTC TTGTGGCCAG 2040 TGCCCTCTTT GTGTTTTATC ATGAACCTGC TATGTGCCCA CCTCAAAGCT GGACACTGTG 2100 GTTCAAACAT TTCCTTCAGG AAGCCACTAG TCCACTTCCT GTTAGAAAAG ATTCTGAACT 2160 TCTTTCCCAG ATAAGTTGAA GAACCTGTTT TCTGACCTGG TTAGAAATTG AAAACTCAAT 2220 CGAAAGATTG GCAAAGAAAA TTGTGGAAAT CTATGAAAGT AGAAAAAAAT GAAAAATACA 2280
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