| Tag | Content |
|---|
EnhancerAtlas ID | HS118-16674 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr6:142579470-142581290 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr6:142580910-142580925 | AATGTCCAAAGTCCA | + | 6.09 |
| | | 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 |
| GH06I142259 | chr6 | 142580184 | 142581298 |
| Enhancer Sequence | GAATTTCCAG AGGCATGAAG AACATGATGT CTGTAGACGT CAAGACTGGA AGGAATTTTC 60
TAAGCATAAA TCTTGGTCCT ATGATGTTAC AGGCCGAAAG AATGAGGGTC GTGATCAACT 120
CAGTATACCA CTGGAGGCTA TATGAGTAAG CAACAAAACT GTTTCTCATA AATGCAGAAT 180
TGTGACAAAC TGACAAAACT GCATCTGCCA TCCAGAAGGA ATGCTGAGGG CAGTCATGCC 240
CCAAGCGCAG TGTTTCTTGT GATTAGGTAC ATCTGAAGCC TGTTAGTAAC AATATGAACG 300
TGTGATCAAT TAAGCAGCTG ACCAGTTGTT ACCTCCTTCT CCTCGCTTTT GTTACCCAAT 360
AAATAGGAGG GGCTGTGGAA GCTCAGGGGT GCCTTTGCTC ACTGGAAGTG GGGAGCTCTC 420
TTCTTCTTCC CCGGCTTCCC TTCCTTTAAA ACAGTTTCTT TTGTTTTTTG TTATAATTTC 480
TAAGTTCGTC CCTTCGTTCA GTTTGTAATG ACGGTCTCAG GCAGTAACAA CAGTAACTGC 540
TATAATGACC GTCTCAAGTA GTAACCGTGG CAGTCGGCCA CATTATGACA GAGCCTATGG 600
CAGGCCAGTC AGTAACATTT TGTAGATGGC TACCTACACT ATTAATTCTC ATGAACTGTT 660
CTTTGCCTCT AGTCTTTACC CTATTCCAGA ACTAGCGAGT TGATTGCATC AGTCTCTGAG 720
TAACATTTTT TAAAACTTGA CAATATGCAT TGACAAGGAG TTTATCTAGT TAAATAATTC 780
CTATTTAAAT ACCTGGTTAA TGATATTTGG GTCTTATATC TACCCTCAAA TCAATTTTAT 840
ATTTTTAATG ACACTACAGG TCAATTCCTT TTAAGAAAAA TTGGCAAAGA AATATTTTTA 900
TGTTTTATTT GGATAATGGT CCCAGAGAGC CCTGGCACAC ATTTTGACAG AGTGAAAAAG 960
GTTCAGGAAA AAACCCACAA GCATAATGAA AACAGAGGGG AAAGGTAAAA TCAACAGTAA 1020
GTCTTGGATA GAAGTGAAAG TGTGACCATT TGCAATAGCA AAGAGTATAC CTGGCTGTCT 1080
TTCACAATTC ACCTAAGGAG TTGCTCACGG ATCTTGCATG GTGGCTTGAA CTCTAGCATA 1140
TTCCTTCTGA TCCTGACCGA ACAGCAGTCC TCCTCAGTCT CAAGAGCCTC ACATTACATG 1200
TGTGAGGCCC AGTCCCAAAC CAAGGATCTA GAGTCCTTAG GTGCAGCACC CTTCCTACTT 1260
GCTCTTTCTG ATTCCAGAAC TCTGACCTCT TCTTCCTCAG TTCAGTAGGG CCACAGTTTT 1320
CTTTCTGGTT GCATTCTACC TCTTTGTGCT CAGAAAATTT TCTCCAGGCA CAGAGCTAGC 1380
ATGAAGTGAG AGTCATCTCG TGAGATTCTC TTCTGTTAGG GATTAAAGGC TTGCACTGTC 1440
AATGTCCAAA GTCCACTGTC TGGAAATCAT TGCTTCACAT ATTTTGTCCA ATCTTTTAGC 1500
TTTATGTTTT GTATGGGTAA AAGTGAAAGT CATTCCTGTT TGATAAGATT TTTAACAAAT 1560
CCTTGCAATG TTTATAAGAG ACACATCAAA ATACATTGAA TATAATAAAG AGATAGAGAA 1620
TGATAGACTA AAAAAAAGAC TACCAAGCAA AGCTATTGAA GCCTTATTGG CCGGGTGCAG 1680
TGGCTCACAC CTGTAATCCC AACACTTTGG GAGGCCAAGG CAGGCAGATC ATGGGGTCAG 1740
GAGATCGAGA CCATCCTGGC TAATATGGTG AAACCCCGTC TCTACTAAAA ATACAAAAAA 1800
AATTAGCCAG GCGTGGTGGC 1820
|
| |
|
|
|
