| Tag | Content |
|---|
EnhancerAtlas ID | HS091-34185 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:48491980-48493130 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr3:48492378-48492393 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | 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 |
| GH03I048451 | chr3 | 48492861 | 48493010 |
|
Enhancer Sequence | GGTATGTGAC CCAGATTTTT TTTTTTTTTT TTTTTGGAGA TGGAGTCTGT CATCCAGGCT 60
GGAGTACAGT GACACAATCT TGGCTCACTT CAACCTCTGC CTCCTGGTTT TAAGCGATTC 120
ACATGCCTTA GCTTCCAGAG TAGCTGGGAC TACAGGTGTG CACCACGACG CCCAGCTAAT 180
TCTTGTATTT TTAGTAGAGA CGGAGTTTCA CCATGTTGGC CAGGCTGGTC TCAAACTCCT 240
GGCCTCAGCC TCCCAAAGTG TTGGGATTAC AGGCATGAGC TACCACACCC AGCGACCCAG 300
ATCGTTAATG CCTCTTAGAG CCTAAAGAAT CCGGCCAGGC GCGGTGGCTC ACACCTGTAA 360
TCCCAGCACT TTGGTAGGCC GAGGCCAGTG GATCACCTGA GGTCAGGAGT TCAAGACCAG 420
CCTGGCCAAC ATGGTGAAAA CCCGTCTCTA CTAAAAATAC AAAAATTAGC TAGGCATGGT 480
GGCGGGCACC TGTAATCTCA GCTACTCGGG AGGCTGAGGC AGGAGAATTG CTGGAACCTG 540
GGAGGTGAAG GTTGCAGTGA ACCGAGATCG TGCCATTGCA CTCCAGCCTA GGCGACAATA 600
GCAAGACTCC GTCTCAAAAA AAAAAAGGAA TCTGGTCAGG CAAGGTGGCT CATGCCTGTA 660
ATCCCAGCAC TTTGGGAGGC CAAGGTGAGA GAATCGCTTG AACCCAAGAG TTCAAGACCA 720
GCCTGGGCAA TACAATGAGA CCCTGTCTCT ACAGATAAAA GTGAAAATTG GCCAGGCTAG 780
TGGCACATGC TTTGTAGTCC TAGCTACTCA AGAGGTTGAG GCGAGAGGAT CACTTGAGCC 840
CAGGAGTTCA AGGTTACATT GAGCTATGAT TGTGCCACAG CATTCCAGCC TAAGCAACCC 900
CATCCCCCTC CCTGGCAAAA AGAATCTGCA TGCATGAGTG GCAAGTGTAT GCTTAAGCTA 960
TCTTGATGAA TATCAGCTGT CCCATGAACA GGCCTAGCAG ACCATGGTGA CATCTGGTTG 1020
CTGTGGATAT ATTTTGAGTA CTCATTTGTC TGTTTTTCCT GTGCTTTCTC CATCTCCCCA 1080
ACTACATGTT AAAACAAAGT ACCTAAGTAG TTTTCTCTTA CAAAGTTTTC ACGAGATTAA 1140
TTTGGGATTT 1150
|
