Tag | Content |
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EnhancerAtlas ID | HS113-27608 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr4:79401280-79402950 |
Target genes | |
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) |
ALX3 | MA0634.1 | chr4:79402486-79402496 | TTTAATTAGA | - | 6.02 | PRDM1 | MA0508.2 | chr4:79401818-79401828 | TCACTTTCAC | + | 6.02 |
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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: 1 | ID | Chromosome | Start | End |
GH04I078480 | chr4 | 79401313 | 79404420 |
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Enhancer Sequence | TATTTTGACT ATAGTCACCC TGTTGTGCTA GGGAATACTA GGTCTTCTTT CTAAGTATTT 60 TGTGTACCCA TTAACCATGC CCACTTCCCC CCTCCACCAC CATTTCCCAC CCCCACTACT 120 CTTCCCATCC TCTGGTAACC ATCCTTCTAC AACATGGATG GAAGTGGAGG TCCTTATGCT 180 AAGTGAAATA AGCCAGGCAC AGAAAGACAA ACTTCACATG TTCTCACTTA TTTGTGGGAG 240 CTAAAGGTTA AAATCATTGA GGTCATGGAG ATAGAGTGTA GAAGGTTTTA CTCTGGTTCT 300 TGATGGCAGG CAGGGCTGTG GCATAGAGCC TAGAGCTTCA TGGGCTGACC TCTGTGGTCC 360 AGAGGGAGGG CCTGGCACTG AGCATCTGGG CTTGTGAAAG GGGAGAATGT GATATATTGA 420 GGATGGAAGT GAAGTATTTA GTGTACTGCT AGCTCCTGAA CACTCTCCAA AGTTTCAGTG 480 TCTTCATACA GTGAAACTTT CTCATTCATG TAAGAGCCCA AAGCGATCAG TGGGCAGGTC 540 ACTTTCACAT GGTATTTCAG AGACTCAGGC TCCTTTCCCA CTTGTGGCTC CACAAAGGTC 600 TTGAAGTCTT ATGTATGCTG CAGGCAGATA TACTGCTGGC AGAGGGGCAA CAGCTGTGCT 660 GAGTGTCTCC TGATCTGGGC CAGATCAAGG CCTTTCACAT CTATGAAGGG ATTTGGAGGA 720 GCACTGGGAA CAGGTATTTT TGAGCACTTA CCGAATGCCG GGCACCATAC CGTGCATGTT 780 CCATGCATTC TCACTTAATA TTCTATGGAA GAGAGAACAT TATATAAAAG AGCAAATGGA 840 GGCCTGGATA GGTTAAGTCA GTCATCAATG ATTAAGCAGC TAATAAAATG GCAAGGCTAG 900 ATTCAAAGCC AGACCTTTCT ACTATAGCAT GTTTCTTTTC CCATACAGCA AATGCCCAGC 960 CATAACTACA TTGCATCTCA CAGCATGTTG GCTAGAAAAT GTGGTGATTG AAAATTGTAG 1020 GGTTTTCATG AAGCTTTTCT CTGCCCTTGA TTGTGAAAAT AGCTAAATAT CCTTAGGACA 1080 CTACAAAGCA TGATGTCACA GTGGACAGGA AGATGAGCTT CATTCCTAAG ATGAGTAATA 1140 AGCACATGCG GTTTAAGTCA TGACATGTGC TTGGGTAAAA CAGAGAAATC AACTCAGTTA 1200 GGAACATTTA ATTAGAAACA TTCAGCTTCA GGCTCCATAG AGTCCCCTAG CTGGGTCCTC 1260 CTTAATTGAC TATTTTCTGA CACATCCCTG AGGCCCCAGG CTCTAAGTTT CTTCTCCCTA 1320 AATAGGCTTG AGATGTTTTG CAATAGACCC TTCTCTCCTT AAGTGCATTG TTCTCCTGTG 1380 AGCAGTCTCC CTTGTGAAGC CACAACAGCC TTCTCCCCTA AGGGCTCTCT CCAGCACCAT 1440 CTCCATGAAG CCCTTCTCTA GGTCTCCTCT TGATCCTAGT GTCAGTGAAA AGACAGGTAG 1500 TGACACCTCT AGGCCTTCAC CTCAGATGGG CCATAGGAGC ATCACTGAAG CTAGATTAGA 1560 AAAGCTCAAA GGGCTAAAAG CTGCCACTAT TGCAGTGAGG GAGAACATCA TTCTGAAAAC 1620 CTCGCTGATT TTCTGGCTCA AAGTTGACCA TTAAAATCTC TATGAATCTT 1670
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