| Tag | Content |
|---|
EnhancerAtlas ID | HS076-36376 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr20:47230790-47231810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF1A | MA0046.2 | chr20:47230828-47230843 | CATAAATAATTAACC | + | 6.36 | | HNF1B | MA0153.2 | chr20:47230829-47230842 | ATAAATAATTAAC | - | 6 | | STAT3 | MA0144.2 | chr20:47231519-47231530 | CTTCTGGGAAA | + | 6.62 | | Stat4 | MA0518.1 | chr20:47231519-47231533 | CTTCTGGGAAAGGG | + | 6.38 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTGTGCTTAA TGTCTCTTTA CTGCCCTGAA ATGAAAGTCA TAAATAATTA ACCTATAACA 60
TCATACACCT ACTTAAAAAC TCATTACAAT GCCCTAAGTG GACTATAAAA AGAAATAAAA 120
GGACAATAAT TTTTAATGAA ATAATAACTT GTAATAAATT AAATCATATT TCAATAGGCA 180
AATGAACAGA CACAGACACA GGCACACACA GAGATATAAC CAATAGTTAG ATCCTAGCCA 240
ACTTCTACAG AAGAAGTTTG GATGGAAGAG AAGATCAGGA GTTGCGCTAC AACAGAAGGG 300
CAGAAAAATA AAGACACTTG AATATAAATA TTATATTCGG TGTACGGTAA AATCTTACAA 360
AAATATCTTG TTTTGATATT AAATTGATGT CGGTTCTAGG CTAAGATGAT TAAATGGCTC 420
TTCACACAAG AGCGACCAGA GGAGAAGTGA AATTCGTGTG GGAAACAGGA CGGTCTGTCT 480
TATGTGGACT GTCCTGCGCC TTGGAGGCAT CCAGCATTCC CAGCCCCACC CAGCTGAATG 540
CCAGCAATAT TACCAGTCAT TGAGCCAAGC CACCCCCACA TTTCCATACA ACCTCAGAGG 600
CTGTACCTCT CTGGTGAAAA AGCACTGGCC AAACCATGAT AATTCCACTT CCTCTGCCAG 660
CACCAGGCCT AACAATGCGC TTGGGATGCA ATTTTGGCCA AAGTTACAGG CAATCCAATC 720
TGCTGGGGGC TTCTGGGAAA GGGTTCCAGT CTCTTATAAA GAGGCACTAG GAAGAGACGC 780
GTTCTTTCTT TTGCTTTCAC CTCTTGCACA AGGGTGGGAC GCCTGGAGCT GTGGCGCAAT 840
CCTACGAGCT TCAGAGTGCA AGCCTGAGGG TCAGGCCAAT GTGGAGAGCA CAGTGGGAAG 900
TTGAAAAGAA TCAGGGTCCC TGGTGATCCC CACCTCTGTA CCAGCCAAAC CAGAAGTGCT 960
AGGAAGTCCA CTGGATTTCT TGATTCATGG AGACATAAGA TATTGTCCCT ATGATGTAAG 1020
|
