| Tag | Content |
|---|
EnhancerAtlas ID | HS118-00341 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:29564440-29565980 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gfi1b | MA0483.1 | chr1:29565563-29565574 | GGCTGTGATTT | - | 6.02 | | Six3 | MA0631.1 | chr1:29565709-29565726 | AGATGTGATACCCCTTG | - | 6.35 | | ZNF263 | MA0528.1 | chr1:29565184-29565205 | CCTCCCACCCCATCCTCCCCA | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTGGCTCGCC GCCGGGGGAC GGCGCCCCCT CCCTTGGCGC GCAGGACGCG CGGGGGACGC 60
CCGGGCCTCC CGGGACACTC CCTTGGTGGA GCCTGCAACT TTGTGCGGCC TCCCGGCCGG 120
CCGGGACCGC CAGGTGTGTG CTTGAGTGTG AGCGTGAGTG TGAGCGTGTG GCTCCGCGCT 180
TGTCTGCTGT GTGGTCGCGT TCTCCGGGTG TGTTTCGGAG TCTGGTGTCT TTGGTGTGCG 240
TGCGCGTGTG TGTGTGCGCG CAGCTGAATG TATGTATACG GAGCCTGTGT TTGTGTGTCC 300
GTGTGCTCGT CGGAGTGTGG ACGGTGTGTC GGATGTGTGT GCGTGCGCGT GTTCCACATC 360
CCACCCTGAG GCCTGGGATC CTAGACCGCG GCCCCTTCCC GCGGAGTTTC GGGGCCCTGC 420
TCCGGGTGAC CTCCCCCGCC CTCGCCACCG GCGGGGCTGC TCCGCGGGCT CCGGGTAGCC 480
GGGAGACGCC CGGGGCGGGA TCCGAGCCGA GACACGTGCT GGAGCGGAGC CGCTTCCTCA 540
CGGTCGCCAG CCGCAGACAA CTGACCTCCC CGGCATCGCG TTCGCGGCCC TGCTGCTGGC 600
TCCGGTGTCT CGGGCCGGAA CTCCTGTGGC TCCAGCGTTC GCGCCGGCCA CTGGCCAGCG 660
CTTGGGCCTC GCCCTGCAGC TCCGGGGCCA TAGGGCACAG CTTTAGCTTT GACCTCCCCG 720
TTCCCGAAAG GACGCCCAAG GCGACCTCCC ACCCCATCCT CCCCAACTTC TCCCCCATGT 780
CCTGCGGCAA CTTTGCCTCC CTCTCCCACC GTGAAATCAA ACCCGCGGGG TTCTGTATGC 840
GCCCCATCCC CGCTCCTACC ACCATCGCTT TGATTTCAAG AACACTCACA AGCCCCAAGC 900
CCTGCCAGCA GGAGGACTGT CAGGAACTGA AGTTTGGGAG TGAGGCCTAG AGCAGGTTAC 960
TCCCATTCTT GATGCCTCAG TTTCCTCTTC TGCCTCATAG CCATCATGAT AATGGTGTAT 1020
GGCACTTTTG GTAGATACCA AGTACCTTGT AAAGTAAGGC TCTGTCTGTG AGTGCCAGGG 1080
AACAAAAAAT GGATTTGAGA GTTGTTGCAA AGCCCCAGAC AGAGGCTGTG ATTTAAAGCT 1140
GGGGTATTAG GTGTCAAATT CTGCCTCTGC TACTTGCTAT TCATGTGATG TCTGGCAAAT 1200
CACCTCACTT GTAAAGTTCC TGGCCCCCTT TGTTATTCTT AGAGATGAAC TCAGAAGCCC 1260
AAGTAGAATA GATGTGATAC CCCTTGTCCC CAGTCTGGAC AGAGTCAGCC CAGCTCCCTG 1320
AATGGCTCCG GAGCTTCCGG GTAGGGGCGG TGTGTGATGC CTTCTCAGCC TTGCAAACCT 1380
GGTAGTTATT TATTCTGCTG TGTTCTTGCT ATTTTGTCCT TTTGGTCGCA GGAGTTGTGG 1440
ACGGCAGGAA TGAGGGAGTG GCTGCCCAGT GGTTTCAGGT TGGGCAATAA AGGCTTGTCT 1500
GGGCATCCCT CCCTTTTCCC TGGGGCTAGG GGAGGGGACT 1540
|
| |
|
|
|
