Tag | Content |
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EnhancerAtlas ID | HS147-00812 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:26666020-26667000 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:26666233-26666254 | AAAAAAAAAAAGAAAGAAAAG | - | 6.41 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGAGGTCAG CAGTTCGAGA CCAGCTGACC AACATGGAGA AACCCAGTCT CTACTAAAAA 60 TACAAAATTA GCTGGGCATG CCCGTAATCC CAGCTACTCG GGAGCCTGAG GCAGGAGAAT 120 TGCTTGAACC TGGGAGGCAG AGGTTGCGGT GAGCCGAGAT CATGCCATTG CACTCAAGCC 180 TGGGCAATAA GAGTGAAACT CCGTCTCAAA ACAAAAAAAA AAAAGAAAGA AAAGATATAT 240 AAATAGCCCC CCTTGGACAA CACCCCGCTT CCCCAAGTCC ATTTAGCCAA GGCTCCAAAT 300 AGCTTCTGAG AAAACCTTTG TAGCCATTCC CCCAGAGACC AGGAAAGTGA CTAGGGTGGT 360 CTTTGCAAGG TCAGCCAGCC AAGCCTAAGA CCAAAGCCTG TGCTGGTCCT TTGCTGAACC 420 TTTGGGACCT GGGACAGAAG TTCCCGGGAG AACCTGCAAA GTGCCAGGCC CATAGCCTTG 480 CCTCTGGGTA GCCTGACTTC CAGCCTGGTG GGAGGATGGG CAAGATGGAC AGCCACTTCC 540 TGAGTTCCAA CTTTGACTCC TTCTTTAGGT ACGGTTCCTG CCTCTGTCCA GACTGGCTTT 600 GCCTGCACGT CATCCCAGGA AGCAGCAGAT CCTCTTTGTA TTCTGAGTGT TTCTTCCCCA 660 CCAGGACCAT TTTCATTCAC TCACTCATTC ATCAAATATG TACGAAGCAT CTACTGCATG 720 CAAGGCACTG TGCTAAGGTC ATGTCCTACC CTATCTCATT TAGTCCTCCC AGTGGGCATT 780 ATTCATCCAG TCACAGGTAA GGAAAGTGAG GCACGGAGAA GTTAAGCAAC CTGCCCAAGG 840 TCACACAGCT TGTAAGTAGC AGAGCAGTAT AGTTTTTGTT CACTGTTGCA ACCCAGCACC 900 TCCCATGTGC TTGGCATACA ACAGGCACCT AATCAATGCT GAATGAATCA AAGGAATCCA 960 GAAACATCTG ACTTCAAAGC 980
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