| Tag | Content |
|---|
EnhancerAtlas ID | HS091-49728 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chrX:103380880-103381760 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chrX:103381277-103381296 | TATCGCCACCTGGTGGCTA | - | 7.67 | | Gfi1b | MA0483.1 | chrX:103381163-103381174 | AAATCACAGCT | + | 6.14 | | HSF1 | MA0486.2 | chrX:103381355-103381368 | GAAAATTCTAGAA | - | 6.71 |
|
| | 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 |
| GH0XI104135 | chrX | 103380264 | 103381850 |
|
Enhancer Sequence | CATACATATT ATATATGTAT ATATGTCTGA CATAGTGCCG GAAGTCTCAA AAGATGTCAG 60
TTTTGCTTCT CCCCTCACCC CTTTAACTCC ATCATGGGAG GCATAGCAGA GGAAACGGCA 120
GGTCAGTGAT GTAAGAATTA GAAGCCCAAC AACTGAAGAA CTGGAAACAG CATCATTTCT 180
GTCCTCTGTC TGGTAATGAC AGAATGGCTG GAGCACTAGG CAGCTCCAAA ACAGCCTTGG 240
GCAGGAACGG CAGTGCTCCA AGACCATCAG AACAAAGGGA AAGAAATCAC AGCTTGAACT 300
TTCGTGGACA GGAGAAAAAA TCTGACGTGG ACAGGAACAT GGACTCCTGG CTGGAAGAGG 360
GCTGCTCCTT TCCTCCGCTA CTTGAATCCT TCTGCAATAT CGCCACCTGG TGGCTATCTA 420
GCATCCCTTT ACTTAATTCC CCAGTGCAGT TTGCTCTGAC AGCCCACTGC ACTGTGAAAA 480
TTCTAGAAGG GAACAGCCTC GCTCAGTGAA CTGTTTCGGA ACTGCTCAAA GTTAATCATA 540
TCCTTCTCCA TGTCCTGCAA AGTGTCTTGT ACTCAAGCTC TATTATAGCA CCTCTCATTG 600
TATTATAAAT GTTTACCTGT ACGCATTCAT TCATGCACCC AACAAATTTG TAAGTGTCGT 660
ACCTAGAACA GACAGGCAGA GGAGAAACAA TGATGAACAA AACCAGTTGA CCATGTAAAG 720
AATTAAACAT GTACACAGAG AATTAAAATA GCCATATTTC CAACCACTAT AAAATAATTA 780
TTATAATATT TAATATTTGT TGAGCACTGA ATACTGTATC TGTATTATCC CATTTAATGC 840
TCACAACTCA GTGAGGTAGA TAATATGATT ATCCTCGTGT 880
|
