| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01093 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:145704390-145705640 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA(var.2) | MA0072.1 | chr1:145705465-145705479 | CTGACCTAATTTTG | - | 6.31 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAATTTCACC GTAACTGCTC CTTATCACTA GAAGTCTTCA AGGAAGGACT GAAGCAGAAC 60
CTGGCAGTAG TGCTGGCAGA CAGGAAATAC AAATTCCAGC TCTATCGATG GCTGTGTGAC 120
TGTAAGCAAG TTACCTAACT CCTTGGGCAG TAGTTTATTC ATCTGGAAAA TGAAAATTAA 180
GGGACTAAAT AATATGCTCA AAGCATCCAT TAATTCATAG GTTTATTTGT TCCTCCACTT 240
AACAAATATG TTTAGGTATT CACTCTGCCA AGCCCTGCTG GGGCTGTGAG GACTAGGACG 300
TGAGCCCTAC TGTCAGAACT TTTTTTTCCC CTAACCATTA GATGACCGGG GATTTTTAAT 360
TTAAAAAATT TTTTTTTAAA ACAAGGTCTT GCTGTGTCAC CCAGGCTGGA GGGCAGTGGC 420
ACAATCGTAA CTCACTGCAC CTTTGAACTC CTGGGCTCAA GCAATCCTCC TGCTTCCGCC 480
TTCCGAATAG CTAACACTAC AGGTATGCAC CACTATGCCT GGCTAATTTT TTATTTTGTA 540
GAGACAGATT CTCACTATGT TGTCCAGGCT AGTCTTGAAC TCTAGGCATC AAGCAACCCT 600
CCTGCCTCTG CCTCCCAAAC TGCTGGGATT ACAGGCATGA ACCACTGTGC CTGGCCACTC 660
TCAGAGTTTA AAGCCTAATG TAAAAACAAA TTAGCAAAAA GTTACAATTT AATTCCACAG 720
TTATTATAAT TGAGGAATCT TAGAGATTCC TGAGTCTGAA GCATCAGGGA AACTTCACAG 780
TGAAGTTAGT GCTGGAGCTG ACTTGAAGGA TGAGTAAAAG TTTTTCTAAG AAATATAGGA 840
TGAGAGAGAC CACAGAAATA CCAGAGATGA TTAAAAACAG CCACTGTGTG GAAATGGAGT 900
GAGAATGGAC TGGAGAAACA GACTAATTAT TGAGGGACCA TTGATATCCA AAGACCATGA 960
CTCTGATGGT GCCAGTCTGC CCACTTGATT TTCCCTGTAA GTAATCTGTA ACCTGGATAC 1020
AGAAGTGGAG AAAATAGTTG GGTTAACCCA GGATGTTTTG GCTCGATGGG TGTCTCTGAC 1080
CTAATTTTGC AATGCATTGG CCCTGCCAAC TTTGTACTGC CCCTCACTCT CCTCAAACTT 1140
CACTTCCTTC TGTAGTTTAT ATTTTGTAGT CCATTATTAA TAATCTCTCC CTTATATCCA 1200
CCCTCAGCTC CCTTAGCTTT ACTCCTACTG TGATGGATCC TCGCAAAACC 1250
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