| Tag | Content |
|---|
EnhancerAtlas ID | HS118-01194 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr1:156165960-156167380 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Stat6 | MA0520.1 | chr1:156166542-156166557 | GTTTCTCTGGAACAG | - | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 156166400 | 156166662 | | chr1 | 156166962 | 156167058 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I156196 | chr1 | 156166255 | 156169523 |
| Enhancer Sequence | ACAGGTATCT GCAAAGAGGA TTTTTTCAGA GGGTAAAACA AGAAGAATGG GATTGATATT 60
TCCGCAGGAA GTTTGGAAGT TATGTAACAG AGCAGGTTGA GATCCTACCT TTTAGGAGCA 120
GCCTGCCCCT TTTGAAGGGG TAAAGGGAGT GGGTGCAGTG CCCTCTCTTC TGTTGTAGTG 180
GCTTATCCCT CTAAGGCATG ACCCTTGGAT AGGGGTTACC TGCCTCGGAA AGTCCCCACT 240
TCCTTGTGGG AGTTTAAAAT AGATTGGCAT ATGTGAGAGA TGGAGACAAG GTGGGAAATC 300
GGATCCTGTC TTAGGATTTC TCATCAGGAG ATGCTGATAC TTGGTGTTTC AGCTTGATAA 360
ATTGAGAAGG TGCCATGAAA CCAGGTCCTG GAACAGAATC CCTGGTTGCT CTGTCTTTTA 420
GCTGCTCTGA CCCTCTGCCC TGCAGAGCAT GCATTTTGCA TGTGCCTGGC AGGAGGCCCT 480
CCTGCTTGAG CCCTGCTGTA TTTGTCTGTG TTGACAACGT GACTGCCAGC CATTAAGCTT 540
GGTCAGTCCA CAGACACACT AGGAAAGCAG AGGCAGCTCT TGGTTTCTCT GGAACAGAGC 600
TGCAAGAAGT CTCTGGGCAT CTGCATGGCC AGGAGCTTAT GCTTAACTGT TGAGTGACCT 660
GCAGCCATAA GGGCATTAAT TCTGCCTTCC AGAGGTGGGA ATGACTTGGC TTTAAACAGT 720
GATTTGTGTG AGAATTCTTC AAATCCCATA AGGTAGAAGG CATGGTGGAG TAGAGGAGAA 780
ATCTTGGCTC ATATCTGCCT CTTCCATTGA CCAGCTGTGT GACCTTGGGC CTGTTACTTT 840
TAACCTACCT GACCCTCCAT TTCCTCATTT ATCAGAAGTG TCTAACTGTA CACAAGTTAA 900
ACTGTAAGGA TTACATGAGG TAGTAGTCAA TCCTGGTGTT TCTCTGTATC TTCTCACTTC 960
TCACTGGTGT TGGAAATATG ATCTTGCGAC CCTAGATGGC AGCCACTCTG GGGCAGAAGA 1020
GACAGTGACC ACCTTTTGAA GAGCTCAAAG GAGAATATTG CCCCACAGGG CTTAGTGGGT 1080
CCCCCAGGCT GAGGCTGGGG AGGAGGGCCA CCTTTGCCTA CAGCAAGTGG CATATCATTG 1140
TTCTAGGGGT TCTCTTGACG GCAGAACTTT GCCTCTAGCT CATTTTCCAC AGCCTAGATT 1200
TTCCAATCTT GCCAATCCAG TTGACTTCTG TCTTCTCATT TCCAAGCCAT TGTTCTCTCT 1260
CTTTCACTAT CTACATGGAT TATCCTTCAT TCAAACTGCT TTGTCCCGGC TGGGTGCGGT 1320
GGCTCATGCC TGTAATCCTA GCACTTTGGG AAGCCGAGGC GGGTGGATCA CGAGGTCAGG 1380
AGATCGAGAC CATCCTGGCT AACATGGTGA AACCCCGTCT 1420
|
| |
|
|
|
