Tag | Content |
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EnhancerAtlas ID | HS103-00807 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr1:67798280-67799790 |
SNPs | Number: 2 | 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: 2 | Chromosome | Start | End |
chr1 | 67798444 | 67799772 | chr1 | 67798461 | 67799300 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I067332 | chr1 | 67797898 | 67799828 |
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Enhancer Sequence | GGTTGTTACT TTTATAATCC AGAGCTTACT CATAATATCG TTTTATTATA TATAGTCAAA 60 GTAATTTTTT TAAAGACTAT CTCATGAATT AGATTTTGTT TATATATGTG GTACAGATAA 120 AACTTCTGAA AATGGGCTAT ATTTTATATC CAAGTTCAAG GTAGTAAGTA GTCTGAAAAA 180 TATTTAAGTT ATATCACATT AAGCTAAACT ATAAACTAGG GAAACTCTGG GCTTGTGAAT 240 TCTTGTCATT CTTACTCACA TATGATAATG ACCTAGTTAG AGATGTGTGA AAAGGTTTTT 300 CTTTTCTTTT TTAAAAAGTG TTTGTCTTTT GAATTAAAAT TCCTTCAAGG CAGCACAGTA 360 ACTTTCTTAT TTCCTATAAA ATAAACCACC ATCATAACAA TGAGTATAGC AACTCATTAT 420 GGTTATGAAC TCATGGATGA TTATGAATTG AACCTAGGAA GCTGGCTTAT TCAGTCACTG 480 AAGGTATTCA TAAAGAGAGA AACCCATACT CTGAGATACA CCACCTTTAC CAAGCTCTGT 540 TGGCTTCCTT TCTGTCTCTG AATCTCCCTT TTCTATGTTT GATTTTTCTG TGGGTTGTTG 600 TAGGTCTTTT TTCTCTTACT CTAGGCTGCT TGGTTTTCAC CCCTTACCCG CTGTTTCTGT 660 CATCAGTTTC TTTATGAAAC ACCAACTGAT GTAAACGTAA AAGGTGTGAA TTTTTTTTAA 720 CACGTCTTCC TTTTAACCCT TTCAATGTGT ACTCATATGT AACTTGGCAT TTAAAAAAAA 780 TTAATAGTAA GCTTTTTTTT TTTTTTTTTT AGGTACTCTC TAAAACTGTG AATGACTCTA 840 CAACAGAGTC AGCCTTTTTG CAGCCTTTGC TTCTCAAAAT TGAGAGAAAT GTAACATCTC 900 CGGGTGGATT GGTGTAGTTG TTTATATCAT TTGAACAGTG GGTTAGGGCT TCCTTTACTC 960 CATAGGGCCC TTTACTATGT CATTAAATTC AGCTCCTATC ACTGAAAAAC ACTTTTTAAA 1020 TGACCGAAAA GTAAGGGATA GGAGGAAAGA AACTACTTTG CTGTGTTTAA GAGAACAGTC 1080 TTGAAATCAG CATCCATCAA AGGCAGGCCT GATAGTGACA CTGGGAAGAG AGCAGCCACA 1140 TTTTCCTTGT AGTGGGAAAA CATTCTTGAA TTTGAGCTCA AGGTGTCCAG ACATGCCTGA 1200 GAACATGCAC AGGTATTGAG GGAAGGTGAT CTCTCACCAC TTAGAACACC CAGGAAGAGA 1260 TGCCAAAATA CTGATTAATC AGCTATTCCT TAGAGCTATG TTACCAATAT GTCTCTGTCT 1320 GTTAATCCGC CATTTTAAAA AGTCTTATTT GCAGTTTGTG ATCTTGCTCA ACTCTATTAC 1380 AGCTAACAAA GGAATCGTTG CATGTTCATT CGTACTTTGG AGGGGCAGAG TGGTAAAGGA 1440 GAAACCTTCC CCCATCATGG TGACAGCAAG GGTGAGGGGT GAATAATCCC TAAAGGGGGA 1500 GAAAATGAAG 1510
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