Tag | Content |
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EnhancerAtlas ID | HS176-02712 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr1:170172860-170173920 |
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) |
IRF1 | MA0050.2 | chr1:170172931-170172952 | AAAATGAAAGGGAAAGTCAGC | - | 6.78 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 170173210 | 170173383 | chr1 | 170173777 | 170173860 |
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Enhancer Sequence | AAGGCCATGG TTCATAAAGA TTCTGAGCTC AGAGTAATGG ACTCATGGGT TCTCACAGAA 60 CTAGTGAGGA AAAAATGAAA GGGAAAGTCA GCATACACAC ACACATGCAC ACACACCCCA 120 CCCCTCAGTC TTTCAGATAG GGTCTGTAAC AGTAAGCCAA GGTTCACTTA CAGAGTTCCC 180 ATAACAAATG AGCATATGGT GAGCATTTGA CTGAGGGAAA TACACATCCT TTAAGGAAGC 240 TCTTAAGTTC TCACAAATTC AATAAGAATA GAAGAATGTC TTAAAAATCA GAAGACATCA 300 GAGACATAGA GAAACTCTCA GTAGTTTATT CTTTTTTAAA ACTTGCAACT TAGAGGTGTA 360 TGTCTACATG TAGCCCTCTG AGTTAGGATG CATTCCTCCA CACTACAGCC TGGAGAAAAC 420 AGATCTGCGT GTCCTTTAAT CCATGATCAT TGTAGATCAA GTTACCTCTT TGAAAGAACT 480 TTTCTTTCTC TAGCCAACTA AATGAAAAGA AAATGATGTA CTTAATTGTT TTCTAAATTG 540 CAATTTTTCT CCCACAGATG TTTTTTATCA GTGTTGAGCC CAATGGGCTT TGTCAGTCAC 600 ACGGGGAGAT GAAATCATGT GGTAATAAAA GAGACGGGGT TGGGGGAGGA AGGGAAATAC 660 CATACAGTAT ATTGTCTAAT TGAAAAATGT GCCACATAAA TGCTGAACTT GAAATCTTTC 720 CCTCCCCAAG GGCTACTCAC AACAAACAAT GCACACATCT TCTGCACTGG AAAGATTAGA 780 CTTCTCCCCT TTCTCCATTA TTAATTCAGG CCAATGCAAG AGTTTCCTTT TTTTTTTTTT 840 TTTTTGCCTT TTTTGGGTTA AGTCGTTCTA CTGGAATTGT GATGCAAGGT AACAAGATTC 900 CAAAGTGAAA TCTTAAATGC AAAGGTAATG GCATCTGAGC TAGAGGGTGA AGGTTACAGT 960 GATGATGATA AAGGGATAGC ATTAGATTAA ACTCTAACTT TGTAGAAGGA AGATGAGAAC 1020 TAGCAACAAT ATCTATGAAT GTATCTGAGA AATGGTTGCT 1060
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