Tag | Content |
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EnhancerAtlas ID | HS187-21775 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:134961480-134962640 |
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) |
CTCF | MA0139.1 | chr6:134962251-134962270 | TTCTGCCCCCTGGTGCTCA | - | 6.15 |
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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: 2 | ID | Chromosome | Start | End |
GH06I134640 | chr6 | 134961461 | 134961670 | GH06I134641 | chr6 | 134961689 | 134964507 |
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Enhancer Sequence | CTTACAAGGC TCTTAATGAC AGAATGGTTG GCATAGCCTT ACTTTCCTAA ATAGTTTGCT 60 GATTCACTTG TTCCATTTTT AGACATCAGC AGATCGGCAT TGGTGACATC TGCTAATTAT 120 TTGGTTTGAC TCGTGACTGG CATGAGACTT CCATCTGCAT CAATCAGTAA GACATGATTA 180 GTGTGAGGTT AATACCACCC AATCCATGAC CAATTTGTTG TAATGAGAAG CCTTGTTTAT 240 TTATCGGTTT TCCCCAGAGG TAATCATTTG TTGGAAACAT AGCTGCCAAA AGTCACATTG 300 TCTTCGTATT AATAGCTTAT CAACTCTCAA ATTGCATTGA CCTACCCAAT TACATATTTA 360 AGACCTTCTG CACCTCTCTT ACGGTTTCCA CCTCTCATTT CTACCTGGAA ACAGTCTTGG 420 AAGACAGCTG AAGACTGTGC TTCTATGGTT CGTCCTTCCT TGTTTCCCTA GTACAATATT 480 TTGAGACATC CCCTCAAATG GCCCTCTTCT TTCTAAACCA TCATCATGTG ACAGTCACAG 540 CTTCATTAAG ACATGTTAGT TACGCTTCCT GGTTTAATTC AGAGTGAATT AAATCATACT 600 CAATAAACTC ACCAAGAGTT TTGTTGGTTT CTTGTGTAAT GCTTGGGTAA GATTAGAAAG 660 GCAATGACCT CCAATCATGG TAGTAGCTAA TTCCTTGTTT AATACTTTAG GTCAAAGTGA 720 GTGCACATTT CACCATTTTG TGGTCTACCA GAGCAAACAC AGAAGAATGC TTTCTGCCCC 780 CTGGTGCTCA TTGTCTGCTA CTGCAGCAGA TGAGTCAGCT GAGATATGTT CCAGACAGAA 840 GCAGAAGGAA TTGTGTCTCT ACTGCTTATA GCACATGAGC AAAGCCACAA CTTTTCAGTG 900 CGTCACATGT CAGATACCTC CTAAATATGC AAGTGTCAGG GAAATGAATG AAGAGGATCT 960 CTCAATTCTG TAACAGGAAG CACCACTGGG GAGAATGGCA GAGGCTCTGG GCTCTGGCTC 1020 TTGTTGCTTC ATTAGCCTCT CATCTGGGAG CCCTCTGGGG TGCTGGCTGG TCCACCCTGG 1080 CCATGTCTGG GTCTCTTGAT TATGCCAGGT TATTCCCTGA CTCAACACAC TGACATGTGC 1140 TTCTCTCTCT GCCTAAAAAC 1160
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