| Tag | Content |
|---|
EnhancerAtlas ID | HS118-19982 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chrX:37966020-37967630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chrX:37966578-37966593 | ATGGGGCAAAGTCCA | + | 6.02 | | Hnf4a | MA0114.3 | chrX:37966579-37966595 | TGGGGCAAAGTCCAGG | + | 6.53 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH0XI038106 | chrX | 37966093 | 37966905 |
|
Enhancer Sequence | ATGCGTAAGC ACATAGCATG TTCCTCAGAC TATTTCAGTC ACTGCCTTTT TTGTCTGTAT 60
GTGTGTTTCC TTTTCAAAAG AGTCTTAGCA TTCTTCTTGA TTCAGTCTTC TCAGAGAGTT 120
GATTGTCATG TTCCTCCTAT ACCACACTTT TAAATATTCT CTGAAGCAAA TGTATACTGG 180
TTGTGTCTTT GATTAACTGA TTTTTAAAAC ATAATTCAGG ATTGACATAT TTGCAATTTA 240
CACAGAGGCA GCTCTTTGAA GTAGAATGCT GACATGTTGG CACACCCAGG ATGTACAAAA 300
GCATCTTGTC GATTTCTGTT CTGGGAAATC CTCCAGAGAA AATTACCAAA CTGTTACCCA 360
ATTAAACAAC TCAAAAGGGC AATTATGAGG CTCTCAGGAT TCTAGAGATC AGCCTGGGAG 420
GGCAGGTATG GACCATAGCA CACTGGAGAG AAGCTAGATA TAAAGGTGTG TCAGGGGTTC 480
TCAAGACCAC TGCCAGGTTC AGTGATTCAC TAGGAGGACT TAGGACTCTG CACGCAGTTA 540
TAATCAGCAA AGAGGCACAT GGGGCAAAGT CCAGGAGAGA TCAGGCTCAA GCTTTGCAAG 600
GGTCCTTTCC CAGTGGAGTC ACATAGGATG CATTTAATTC CTCTGGCGAT GAGTTCTGAC 660
AACATCTGTG AAATGTTGTC TGCCAAGGAA GCGTGTTAGA AACTCAGCTG GTCACATACC 720
AAATTTCCAG TCTCTCAGGA GAAAAAGAAC CCGTTCAGCA TAAGCCATAT TGTTTGTACA 780
AACAATTTAG GAACAACGAG CCACTTTTAT CAGTTCTGGG AATGGTGGGA ATCCTGAAAT 840
CCAAGTTGCC AGATGCCACC CAAGGGCCAA ATTTGTAAGC AGGCATTTAG AAGAATGGTA 900
GTCTCAGGCC CACTATGTTA ACTCTTTTCT GCACAATAGA TGACCTAAGT CCAATAAATA 960
ACTCAGTGAA CCTGGTTCCA AATCCCCTAA GATAGACAAA TGAGTGGATT TTGACTACAG 1020
ATTGGTCCAC CTGCCTCCTC AGCTACATTT CAGAGGGCTA CAGGACCAAT GTAATTATTT 1080
TGACTGGCAT GGAAAGGGGT CTTCTAAAAC TCAACAGATA TTCTGTAGAA CTTTGGTAGC 1140
ATCTTATACA TTTCAGCTTT GTACACATCT TGTACATTTC TGAGTCTGCT GTGATACCCT 1200
GCTTCAAGAG GCTCCTGAGA TAGCTCAAGC TAAAGTGTTG GGTAGAATTG CTATCACTAC 1260
TTCAGGTTGT TATTTTTTAT TTTGCCTTTT TCACTGTTTT CTTTTACTCA CCCATTACCA 1320
TTGACCCCAC TCTCTGACAT CAGAAGGCAA GACTAGTAAT AGAGAAGCAT CTAATCCCAG 1380
AAAAATTTGT GAGACCATTA ATATTAATAG TGTATTACAT GTATTGAGTA GTACAATATG 1440
GTAGCTCCTT GGATGTGTCA ACTAATTTAA TCCTCACAAG GCCATCAGTT AGACAGTGTT 1500
ATTTTCCCAG TTTTACAGAT GAAGAAACTG AGGCACAGAG TGGTTATTTA GTAAATTCTT 1560
GAGGTCACCA AATCTCTGAG GCATGGAGTG ATTCAAAACC AGGTGGCTTG 1610
|
