| Tag | Content |
|---|
EnhancerAtlas ID | HS108-11861 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:31698190-31699630 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CEBPA | MA0102.3 | chr14:31699102-31699113 | TATTGTGCAAT | - | 6.62 | | SPI1 | MA0080.4 | chr14:31698457-31698471 | CACTTCCTCTTTCC | - | 6.1 | | ZNF263 | MA0528.1 | chr14:31698923-31698944 | TTCTCCCCACCCCTCTGCTCC | - | 6.25 | | ZNF263 | MA0528.1 | chr14:31698926-31698947 | TCCCCACCCCTCTGCTCCTCC | - | 7.16 |
|
| | 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 |
| GH14I031228 | chr14 | 31697367 | 31699956 |
|
Enhancer Sequence | TAGCAAAATC AACCTATGTC CTTTCATTAA TGGTCTGGAA TCTTATTAGC AAACAAAATT 60
TGCAGGTGGC TTTTATGTTA CTGTTAGTAT CACACTGTGT ACAGAGGGGA CATGGAAGAC 120
ACTAAAAATA ACTAATCTAA CCTCAGTAAA TGTACTGCAC TATATGGGCT GAATATTCTC 180
ACAGACTTAA AGCTCTGAGT AAGATAGTAT TCATTCCTAG AACAAATGAT AATTGAAATC 240
TTTATTCTCT TCTCTTTTAG GGTTCCCCAC TTCCTCTTTC CCCCTAACCT GGGCATAGCT 300
ACAGGGTTTG TGTGTGTGTG TGTGTGTGTG TGTGTGTGTA AAGAAATGAC TTGTAGTCTC 360
AAAAAACTAA GCACAGAACC TTCTTTGCAT AGTGATTTCT TCTATCATAT ACATTCTATA 420
TTGTCACATT CATGAAATTA CAACAGAATT TGTAATAATA CAGCAATGGC TGTTCTCCAT 480
TTGAACTATT TTAGTCACTG AAAAAAGTGT GGTGCCTCTG TCAAAGATTT ACTTATATAT 540
TACCAATGGA TTAATAGAAA TATATTGAAT GTTGATTAAT TTGTTTCTTC TAGTTCTTTA 600
ATTCTAATAT TAAGTTTATT TGAAGCTACA ACCCATAAGT GTCCAGCTTT TCATTTCTTT 660
CATAAATAAA GCTGGAAGTG ATTATAAGTT CATATCCTCA TTTGCTTCTG ATTGATGCTT 720
CCTTATAGGC TCTTTCTCCC CACCCCTCTG CTCCTCCCCA GTGTTACACA ACACTACGGA 780
GCCAGGAACA CAATGTCAAC TGTCAACGTC TTTCTAAAGG CAGTGGGTGA TATTTACACA 840
CGTAAGCTGC TGGCACTAAC AAGGTGACTG GAGTCAAATG TAAACCACGG GTTTATCATT 900
CCCAGTCAAA TATATTGTGC AATGGGGTAG CAATAGGCAC TGTGTGAAAG GTTGCCTAAC 960
AAGCCGCCAG CCTTAGGATT AGTCAGCTCC TTGCTGTGAG ATGTGTGTGA GCGAGATACT 1020
GGAGGTCTCT GGTGATAGAA AAGCACGCTG GCCAATGGCA AGAACCAAAA GGAGGGGAAA 1080
CTCAATTTTT TGGCAAACAA TTTGAATCTT AGCAAAAGAC CTTTGTTCTC TGAGGTGCAG 1140
AGGCTGAGAG GTTACTGAGA AACATCCAAG AAAAGGACGT TCTCTGTGAA AACTTCCCCT 1200
CCTATACAAA ACTTTATAAA CTGGTACGAT TTCTGGCCAT TTAAATTTAT AGTGAAATCA 1260
AAACATGTTT CTGGGGAAAT CTTTTTTTTC TTTTCGTAAT AAAAGTTGTA ATTATTATTT 1320
TTTTAAGACA GAGCCTCGAT CTGTCGCCCA GGCTGGAGTG CAGTGGCACT ATCTCGGCTC 1380
ACTGCCACCT CCACCTCCCA GGTTCAAGTG ATTCTCCTGT CTCAGCCTTC TGAGTAGCTG 1440
|
