Tag | Content |
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EnhancerAtlas ID | HS176-12317 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr14:35134970-35136150 |
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) |
STAT1 | MA0137.3 | chr14:35135257-35135268 | TTTCCAGGAAA | + | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH14I034665 | chr14 | 35134268 | 35136406 |
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Enhancer Sequence | CTTACTTGTC TCAATCCCTC AGATTCTAAT TTATTTCTTA TAGAGTAGTT TACTCTTTCT 60 TTACTTGCCC CAAGCCATCA AACTTATTCC CAAAGGGTCT CATTTTTATA ATTAATTTTT 120 AAAATGTGCT CCTAAACCAT AATAGTTCTA ACTAGCACTG GGATCAGTTT TGATTTTTTC 180 TTCCCCTGCT AAATGTACAC CATGATGATG GCAGTAGTGA GGAAGACAAT GACAACAATC 240 CTTAAGCCAA TATGTTTAAG TTATTACATG AAGAAAGACA ATGCCCTTTT CCAGGAAAAT 300 AAATGGTCTT TTCTTTGACA TGTAAGAGAT TTCTTGTTAT ACCCCTATTC ACTACAGAAT 360 AGAAACTAGA GTTTCTAAAG TACTTTAAGC TCTCAAAAAT AAAAATGCTT AACTCTGCAG 420 ATGCATTTGA TAAATGTATC TGTATGGCAG CAAGCCAGCA AGTTCCTGAA CGACAACAGG 480 ATGTAAGCTC AGCTTTATGA AGCATATTTA TTGTCAGAGT CATCACATTC TCTAACAGAC 540 CATGGGGAAG TAAGAGACAT GGGCCGCAAT TTTGACATCA TATGTTTCTG CAATTTAAAA 600 ATGCACCAAC AGCATTTGGG AGAAACAAAA AAGGCAGGAT GTTAAATGTT CACACCAACT 660 ATAAGTTACA TACTCATTTC AGAATTTTAA AGTGAGAACA ATAAAAACAT ATCATGGAAG 720 CAGAGAGCGT ATCTACTTTT TGTTTAGGTC CTCTACAGCA CATTTCTCTA TATCTTGAAG 780 AAAAAGTCAT TTTGCTAATA TTGTTGCTAA ATAAATGCAC AGTAGTCTTT AAAATAGACT 840 TTGAAAAGGC ACCATTCCTA TTAGGTTGGT ATAAAGATGA AATGAAATAA TACATGTAAA 900 ATGCTTAGTG TAATGCTTGA AGCATAATAC TGTTGACTAC TCCACAGAAA TTCAGAAGGA 960 ATCACAAAGA GAAGACTAGG GGATTATTTA TTCCTGGTAT TACTCAATCC AATTCAACAA 1020 ATATTTAATG ATCATCAACT TTATTTTTAT TTTTATTTTT TTGAGATGGA GTCTCACTCT 1080 GTTGCCCAGG CTGGAGTGCA GTGGTGTGAT TTCAGCTTAC TGCAACCTCT GCCTCCTGGG 1140 TTCAAGCAAT TATCGTGCCT CAGCCTCCCA AGTAGATGGG 1180
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