| Tag | Content |
|---|
EnhancerAtlas ID | HS118-10263 | Organism | Homo sapiens | Tissue/cell | Liver | Coordinate | chr2:109637990-109639110 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr2:109638190-109638201 | ACAGGGTGTGG | - | 6.14 | | ZNF263 | MA0528.1 | chr2:109639054-109639075 | AAAGGTGGGAGGGGGAGAGGG | + | 6.17 | | ZNF263 | MA0528.1 | chr2:109639061-109639082 | GGAGGGGGAGAGGGAAGAGGG | + | 6.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAAAAAAGTG CTGACAAAGA GGGACTTTCC CTCAGAATGA GTTCTGACAT GCGATAGTTC 60
TCCTCCAGAC CTGAGGGGTC TGGGGAGAAG ACGGCTGGCA GGTATGGGCA TCGACAGACG 120
TTGGAAGCGA GGTAAAGAGA GCAGAGGAAA GGACACTGGC CTCGCAGGCA GTGTGTGTCC 180
ATTACCAGGT CCCCAGGGCC ACAGGGTGTG GAGGGAGCTG TGAACTCACC TGGGCATCCC 240
CCGAGGTCCT TAAAAAGAAG ACAGCAGAAG CAGACAAATA GCGGTTAAGA AATCCGAACA 300
AAATCGCTTT CAGGATTGTC TTTCCTGAGA AGAGAATCTG TGAGGCACGA TTTTTCACCT 360
TCCACCAGGG ATTGAGAAGT GCCCTGCGGG GTTGAGAGCA ACCCGGGAGC CAAGCAGGAG 420
TGGAACTTTT AGATGGGCCT TGGCATGTGG CTTACACAAG AGGCCCTTTG GCCTGCACAG 480
AGTTTACACA ATTCGAAGGC TTTCTGGAAA ACGTGCCTCA GAGCCGTGTG CCCCAGCTTG 540
CTTGTTATAT CTGGCAGGCA CCGGCTGCTG TGGGTTCCGC ACCTAGGGTG CGCCACACCG 600
TCCCCTACTG CCCTTTAGCC TGTATCCAGG GGCAGTGGCT GGAACTCAGG CAGAGGAGCA 660
GAGGCCCAGG CATGCGAAGT GGGGTGCCTG CAGTTAGGGG TTGGGCTGGG AACGCCAATA 720
CTAAACGCCT CAATAACCAG CAACTGTGGT TCCCCCGCCC CACTCACTCA TGTGCCGCTG 780
CCACAGCACT CCATCTACCT TCCCCAGGGG GAGCAGTGTT ACTGTCCTCA GGCATCGTGG 840
CAATTATGTG GACAGCGTCG CTCATTTGTC CAGTGTTCTT GGGGATCCAG GTGCTCAGAA 900
AGGTGGATTT TCCAGATGGT GGACAGTTCC CTTTTGCAGT GTAAAATCTT TAAAAATTAC 960
TGTTTTTCAG AAAGTCAAAC ACTGCATTTC TCAATTGTAA GTGGGAGTTA AACAATGTGT 1020
ACACATGGAC ATGGAGAGTG GAATAATAGA CACTGGAGAC TCCAAAAGGT GGGAGGGGGA 1080
GAGGGAAGAG GGATGAGAAA TTACCTAAAG GGTATCACAC 1120
|
| |
|
|
|
