Tag | Content |
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EnhancerAtlas ID | HS053-02719 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:159567120-159569010 |
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) |
RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 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 |
GH01I159596 | chr1 | 159566407 | 159569121 |
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Enhancer Sequence | TCCTCAGTCT GGAACTTACT CCTTGCACAT ACCTTTTTCT GCACTGTGCC ATCATCCACT 60 TCTCTTTACT TCCTAACTAC CACCAACTGA AAATTATACA TATAAAAGCT TTAAACAAAG 120 TCTCTTGAGG CTCTCAAGGG AGTTTACATT ACAGTATAGT TCAGCAAACA ATTTTAAATC 180 AAATAGTACA CCTCTTTATT CTTAGAATTC CCTCTGCCAA AAAAGAAATC AGCTACTTTT 240 TTTTAAATTC AAGGTCCAAC TTTCTGTTGT GTTGCTGATT CTCTTCTCTC TTTTTCCAAC 300 GACTTCCACT TCTCTCTCTA GTTTACATGT CTCCAAACCT TAAGCCTCTG TTAATACTTT 360 CACAATAAGT CAATTTTGCC AACGGTTTGC CTCCCCTAGA CCATCTAGGC TGGGCCCAGA 420 ACACCTCATC TTCACTCCCA CTGAAGTGTT CCTGAAGGTC AGCTCTCACT GACCTTGATT 480 CTGCTCCCCT ACACTGTCAC CAGAAGCTAT CCACCTATGG TTCTAATTCA GTAAGTCCAA 540 CTCTCTCACC CCCTTTTTTT GTCTCAGCTG TGTGGGCTTT CCCAGGATGG CATGCAATGG 600 GACCCCTGTG CCATGCATAT TGTAAAGGAA AATGCCTCCC TCCATGCGCT ACAAAACAGC 660 ACATTTATGA TGGCACTTTG AAAAGATATG GGTTGTGGTG TCACATATTG ACAATTCCTT 720 GGCCAGAGGC TTAACAGTGC CAGCAGTGCC AGAAGATTAA GAAGACAGCA AAAACAGAAA 780 AGGGAGAAGA TGGTGAAGTA GTTATATAAC ATGAGCGAGA ATGCTCCTGA TTACAAAGCA 840 GAGAAATTGA CTTTTTTTCT TAGTGTTTTC TATAGTCATT GCTCTATCCC TGTTCTAGAA 900 TTCAAGTCAT GATAAGAATT TCTTCACGTT GACTTCCTGC ATTGCTTTCA GACATTGCAA 960 TTAAAGAATG CGAAGAAAGA ACCTCACAGA GGTAACAGAG TTTGTTTTCC TGGGATTCTC 1020 CAGATTCCAC AAACATCACA TCACTCTCTT TGTGGTTTTT CTCATCCTGT ACACATTAAC 1080 TGTGGCTGGC AATGCCATCA TCATGACCAT CATCTGCATT GACCGTCACC TCCACACTCC 1140 CATGTACTTC TTCCTGAGCA TGCTGGCTAG CTCAAAGACA GTGTACACAC TGTTCATCAT 1200 TCCACAGATG CTCTCCAGCT TCGTAACCCA GACCCAGCCA ATCTCCCTAG CAGGTTGTAC 1260 CACCCAAACG TTCTTCTTTG TTACCTTGGC CATCAACAAT TGCTTCTTGC TCACAGTGAT 1320 GGGCTATGAC CACTATATGG CCATCTGCAA TCCCTTGAGA TACAGGGTCA TTACGAGCAA 1380 GAAGGTGTGT GTCCAGCTGG TGTGTGGAGC CTTTAGCATT GGCCTGGCCA TGGCAGCTGT 1440 CCAGGTAACA TCCATATTTA CCTTACCTTT TTGTCACACG GTGGTTGGTC ATTTCTTCTG 1500 TGACATCCTC CCTGTCATGA AACTCTCCTG TATTAATACC ACTATCAATG AGATAATCAA 1560 TTTTGTTGTC AGGTTATTTG TCATCCTGGT CCCCATGGGT CTGGTCTTCA TCTCCTATGT 1620 CCTCATCATC TCCACTGTCC TCAAGATTGC CTCAGCTGAG GGTTGGAAGA AGACCTTTGC 1680 CACCTGTGCC TTCCACCTCA CTGTGGTCAT TGTCCATTAT GGCTGTGCTT CCATTGCCTA 1740 CCTCATGCCC AAGTCAGAAA ACTCTATAGA ACAAGACCTC CTTCTCTCAG TGACCTAAAC 1800 CATCATCACT CCCCTGCTGA ACCCTGTTGT TTACAGCCTA AAGAACAAGG AGGTCAAGGA 1860 TGCCCTATGC AGGGCCATGG GCAGAAACAT 1890
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