| Tag | Content |
|---|
EnhancerAtlas ID | HS118-09909 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr2:55085100-55086530 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB3 | MA0638.1 | chr2:55085360-55085374 | TTATGACGTGGCAT | - | 6.75 | | HOXC11 | MA0651.1 | chr2:55086460-55086471 | ATTTTACGACC | - | 6.62 | | RARA | MA0729.1 | chr2:55085537-55085555 | AAGGTATAAAGGTCAAGG | + | 6.45 |
|
| | 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 |
| GH02I054858 | chr2 | 55085888 | 55086308 |
|
Enhancer Sequence | TGCTGCATAA CAAATTATTC TCCAAACTTA AAAGTGTAAA TGCACAAACA TTTATTATAT 60
CATGGTTTCT GGGAGTCAAG GAGTCCCAAG AAGCTTAGCT GGGTGATTCT AGTTCAGGGT 120
CTCTCATGAG GTTGCAGTCA TGTGAAGGCT AGACTGAGGC CAGAGGATTC GCTTCTTCCA 180
AGATGGCTCA CTCATGTGGC TCTTGGCAGG AGGCCTCAGT TCCTGCTGTG TGAGCCTCTC 240
CATAGATTGC TCCAGTGTGC TTATGACGTG GCATATAGAG ATCCAAGAAA GACAGCAAGG 300
CAGAATCTGC AGTACCTTTT ATAACCTCCT CTTAGATGTC AGCTTCACTT TTGCCATATT 360
CTGTTCATTT TGTATCAGAG AATTTGTGGA CATATTTTTA AACCTCTGCA AAGAGATAGG 420
CTAATTGATC TGTGAGGAAG GTATAAAGGT CAAGGAAGCA AAGAAGAGGC CAACACTTTA 480
AGATCTAAAG AGAGTTGGGA AGAGCATACC CTGCTCCCCA ATTACTCAAT CATGAGCCAG 540
CATTTCCAGC TGACCTTAGT TGGAGCCAGT TTGACTTTAT TACGAAACTG ATTTAGGTAA 600
CTCTTTGAAG TAGGCAAGTT TGCTTTTGAG ACCCAATGCT TCCTTTCCCT TCTGCAGCAG 660
AATTCCCCTA ATTTTTCTCA GAGCCCCTGA TATAATGAGG CTTATCTGGT CAGAGCATGC 720
TCTCAAAAAA TGTATGAGCA TGACATGTAG CAGTAATTTT CACCTTCTTA CAAATCATTG 780
CCTCTCCAGT GGACATTTGA AATTTAAACA TGTGATAGTT GAACAGATGG CCTCCCCCAA 840
CCCTAATAAA AGGGATTTCA TTTAGAGAAA CTGTGAGAAA TAGAAATGTT TTTGAAGAGA 900
GGTTGGGGTA TTTGACCTCC TGAAATCTAC CATGGACTTT GGGGTTCTAG GCCTCCATGT 960
AAGATGGACC CTGCTTATTA CTCGAGTGCC TTGATGCCGC TGTGTACTGA GCATATGCTG 1020
ATATGCTGAA GGCTTTACTA CTGTAGTTCA ACCACAAATA TCACTTCAAG TAGCTTTTTC 1080
TATTGCACTC ACTACCTGGG GTTAGTGTTC ACTGAGTAAA GCAACCAGTT TAAGGAGGAA 1140
AAAATGATTC TCCAAACTCT ATGTCTACGT GACTCCAAAC AATAATTTTA TTTCCATAGA 1200
ATTATTTTCT GTTTCCCTGT TAAACAGGAT TGCCTGTCTT ATCTTTCATT TAAATAAGAA 1260
TGTGTAAGAT GTTCATTCTC TGTCATTTAT TTTCAGAATC AGTGAAGCAG TAGGCATTAT 1320
TTGGAACAGG TTCAGATGTG TCTTTAGCCA CAGGGCTTAA ATTTTACGAC CTATTTTTAG 1380
CTTACTGCAT ATTGGAATAA TTGAGATATA TTTTGAAGCA TTTGGTTATT 1430
|
