| Tag | Content |
|---|
EnhancerAtlas ID | HS147-03159 | Organism | Homo sapiens | Tissue/cell | NHEK | Coordinate | chr1:150480760-150482000 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Crx | MA0467.1 | chr1:150481850-150481861 | GAGAGGATTAG | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 150481400 | 150482000 | | chr1 | 150481671 | 150481757 |
| Enhancer Sequence | TTGGGGGATC AGCACTTAGG AGGGGGTCTG GGCTTGCATG GCAGGGGTCT GGGTCCAGGC 60
ATCCCAGACG GCTCATCACT AGCAGAGTGA TTCTCCGTTT GGCTTTCCTT TTCTGAGCAG 120
GCCCAAAGTG GGCCTAGGCC AGTGGAGCCT TTAACCAAGG AGGCAGAGAG CAGGGGCACA 180
GAAGGAGAGG GGTTCCTAGA AACTGCTGCC AAGAAACACA GAATCCCAGT CAAATAGACA 240
ACTGAGTGGG GGGTGGGTTC ACAGAGTGAG GGTCTCCTGC TGATGAGGAT GTAGGGAGGT 300
GGCTGGTGGG AGAGGCAAGG GAGGGAAAAG GGGCCCCCAG GCTGCTCAAA ACCGGATTGC 360
TGGCCCAGCA AGCCTCGACT GACTCCCTGT CTGATTAGAG GAGTTGAGGG GTGTCCATCC 420
ACAGACCCAC CCTCCATCCA GCACAAACAC ATTCTTTATC TGCTTTGATG CCTGAACAAA 480
ACAGGAACCC CTCAATGCTA TGGGTGGAAA CTAAGAAAAA AAGGAAAAGA AAAGGAAAAA 540
AACCACCCAG GGCACTCCTG CAGGAAGCTG CTGAGGATGT CAGCAAATCT GTCCACTTCT 600
CTGTGAAGCC CCATGCCATC ATTCTTCCCA GCTCCTGGTC TTTTGTGTCT GCAGATCACC 660
TACAAGTGAC CCTTCCCTGT GCCTGTCCCA GTCCCCCAGG CCCTAAATTG AGACCTAAAC 720
TAAGGCGGAG CTGAGACTGG CTGAAGGGGA AGCACTCAAC CTTCAGGAAG CCTCCTTAAC 780
CAAAGGCCTA AAGATGTTTC AAGGGCCTGG AGTAGGAGGG TGGGTGGAGG AGGTGGATTG 840
GGTAGGCTCC AACCAGCTCA AGGTCCAGAC TTTTTCCTCT GAAAGCTAGA GACGCATCCC 900
AGCAGAGACT GGGGAGGACA ACCCACAGCC CTGAGGGAAA GACTGGCAGA GGAAATGAGG 960
GCCTCCCTCC CCAATCCCGT ATGCCATACT CCCTTTAGGC CCAACCTCTG AGCCAGTAGA 1020
GGTGGAGCTA TCAGACCGCC ACAGGCTTTC TCAGAACCCA GCTGGTCATG TCTAGGTGTG 1080
TTGGGGCTGG GAGAGGATTA GGGGACACGG GGCAGGTGAA TACAGAGGGG CATCTCGTGT 1140
CTTGCTTGTC TGTCCTACAC TCTTGATCTC CACAGCCTCC CCATCCCTTG CTGAAGTCCA 1200
GGGAAGGCCC TCCCAGTGGC CCCTGACTTG CCCTTCTTCC 1240
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