Tag | Content |
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EnhancerAtlas ID | HS095-01298 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr1:67798580-67800210 |
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) |
TBX21 | MA0690.1 | chr1:67798980-67798990 | AAGGTGTGAA | + | 6.02 | TBX2 | MA0688.1 | chr1:67798980-67798991 | AAGGTGTGAAT | + | 6.02 |
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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 |
GH01I067332 | chr1 | 67797898 | 67799828 |
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Enhancer Sequence | CTTTTCTTTT TTAAAAAGTG TTTGTCTTTT GAATTAAAAT TCCTTCAAGG CAGCACAGTA 60 ACTTTCTTAT TTCCTATAAA ATAAACCACC ATCATAACAA TGAGTATAGC AACTCATTAT 120 GGTTATGAAC TCATGGATGA TTATGAATTG AACCTAGGAA GCTGGCTTAT TCAGTCACTG 180 AAGGTATTCA TAAAGAGAGA AACCCATACT CTGAGATACA CCACCTTTAC CAAGCTCTGT 240 TGGCTTCCTT TCTGTCTCTG AATCTCCCTT TTCTATGTTT GATTTTTCTG TGGGTTGTTG 300 TAGGTCTTTT TTCTCTTACT CTAGGCTGCT TGGTTTTCAC CCCTTACCCG CTGTTTCTGT 360 CATCAGTTTC TTTATGAAAC ACCAACTGAT GTAAACGTAA AAGGTGTGAA TTTTTTTTAA 420 CACGTCTTCC TTTTAACCCT TTCAATGTGT ACTCATATGT AACTTGGCAT TTAAAAAAAA 480 TTAATAGTAA GCTTTTTTTT TTTTTTTTTT AGGTACTCTC TAAAACTGTG AATGACTCTA 540 CAACAGAGTC AGCCTTTTTG CAGCCTTTGC TTCTCAAAAT TGAGAGAAAT GTAACATCTC 600 CGGGTGGATT GGTGTAGTTG TTTATATCAT TTGAACAGTG GGTTAGGGCT TCCTTTACTC 660 CATAGGGCCC TTTACTATGT CATTAAATTC AGCTCCTATC ACTGAAAAAC ACTTTTTAAA 720 TGACCGAAAA GTAAGGGATA GGAGGAAAGA AACTACTTTG CTGTGTTTAA GAGAACAGTC 780 TTGAAATCAG CATCCATCAA AGGCAGGCCT GATAGTGACA CTGGGAAGAG AGCAGCCACA 840 TTTTCCTTGT AGTGGGAAAA CATTCTTGAA TTTGAGCTCA AGGTGTCCAG ACATGCCTGA 900 GAACATGCAC AGGTATTGAG GGAAGGTGAT CTCTCACCAC TTAGAACACC CAGGAAGAGA 960 TGCCAAAATA CTGATTAATC AGCTATTCCT TAGAGCTATG TTACCAATAT GTCTCTGTCT 1020 GTTAATCCGC CATTTTAAAA AGTCTTATTT GCAGTTTGTG ATCTTGCTCA ACTCTATTAC 1080 AGCTAACAAA GGAATCGTTG CATGTTCATT CGTACTTTGG AGGGGCAGAG TGGTAAAGGA 1140 GAAACCTTCC CCCATCATGG TGACAGCAAG GGTGAGGGGT GAATAATCCC TAAAGGGGGA 1200 GAAAATGAAG AGTTACCAGC TGCAGCCACC TCTTCCCACA TTGAGAAGCT AGGAAATTCA 1260 TGCACTCATT TGTAATTTAA AAATATTGCC AAGATAAGAT AGGTGTGAAC AATTAAATAC 1320 TAGAGATTAT TTTGGATAGC AAACATTTGA TAACAGTCAA GCTTGGTGGA TTGGCAAACA 1380 TTTTCTCTAC AGGTCCAGAT AGTAATATTT TCAGCTTTGC GGATCATACG ATCTGTCGCA 1440 ACTGCTAAAT GTGCTATTGT CACATGCAAG CTGCCATTGA CAATACCTAA ACAAACAGGC 1500 ATGGCTGTGT TCCAACAAAA CTTTATTTAT GTATGCTGAA ATTGGAATTT TATGTAATCT 1560 TCACATGTCA CTAAAAAGGA TTCTTCTTTT GTTTGTTTTG AGACGGAGTC TGGCTCTGTC 1620 ACCCATGCTG 1630
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