| Tag | Content |
|---|
EnhancerAtlas ID | HS052-00594 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr1:24476040-24477520 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:24477126-24477145 | CGTCCAGGAGGTGGCAGCA | + | 6.27 | | HLTF | MA0109.1 | chr1:24476873-24476883 | AACCTTATAT | + | 6.02 | | STAT1 | MA0137.3 | chr1:24477234-24477245 | TTTCCTGGAAA | - | 6.62 | | Stat4 | MA0518.1 | chr1:24477231-24477245 | CTGTTTCCTGGAAA | - | 6.87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 24476382 | 24476609 | | chr1 | 24476200 | 24477083 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I024149 | chr1 | 24475961 | 24479769 |
|
Enhancer Sequence | TCATTTCTGA GGCCCGATTC CAGGGCTGGA GAAAGTAACG GCATTGCATC CTGCAGGTTA 60
GGCGTCCAGG CTGGGTTAGA GTTACTTAGA AGCAGGGGCT TTCATGAAAG GGCCTGGAGC 120
TCAGAGATGG GAGTGTGGGG GCTCCAGGCT CCTACTGGAC TCTGGCTTCC CAGATGGTCC 180
ACTAAGCACC TGGAGAAACA GACTCAGAGT GGGGTGGGAT ATGTCCCACC CTGGAGGCAC 240
CGCCCTCCTA GAGAGGGGCC TCTCGCCATA TGCTGATGGT TTTGTCCACC AGGACAGGGC 300
ACTCCTCGTG ACCTTATCCT CTTCATCCAC TTAAATAAGC AGTTGGGGGA AATAAAAAGA 360
CTCAGCTTAT ATAAAGCCAT CACACCTCCA TGTCATGTAT CGTCACACGC CAAGGGTGGG 420
GCTCCCAGGG CTGGAACCGG TCCTGGTGTC AACCAGTATC TCTTGAGGAA CTGACTCATG 480
GAGCTGACTC ACGCATTTAG ATATAACTTC TAGTCTGTTT TCTAGAAAAA ACACCCCCAA 540
CCCTCATTAC TTCAGCCCCA CTTTATGCAC ACAGGAATGA GCTCAGGGAA GATGCGCAGG 600
CAGCCATTGA TCAAAACCTA AATCACATGG GAAACAATCA ATTACAGAAT AATAAGTCCC 660
AGACCAAGTG TTAAGGTCCT GTTCTGTCTC CCGCGTACTC CCTCCAACAT CACTATGCTC 720
GCTGAGCAGC ACCAGTGCCC CCTCAGAGCA GATGCTGGGC GAGGGAGGAC GGGCACCGAC 780
GGGCAACGGG AATTTGGGAT CAGGATGGTA TCATCGCATG CGAGAGCTCC TGCAACCTTA 840
TATGTAAGTC AGTCACAGCC GTCCACTTAC TGACTCCAAT TCATACGCCA ATTCACTCAC 900
TTATTCTTTC ATTCACTTAC TCAATCCCAA GCTTCCACTC TGTGCCAGGT GCTGGTGCCA 960
AGAGGAAAAG CAACCCCTTT CCTAAAGGAA GTTTTCAGGG CGTCCATTAC CCCAGCCCTC 1020
CCCTCTCCAG GTTCCCTGAG CTCGGTTCGG GTAAGACCGC GCCCAGCCGC CCTGACATAC 1080
CACCACCGTC CAGGAGGTGG CAGCAGACAG GTTCGGAGAA GCTCAAGGGC GGCGACCCAG 1140
CAGTAGGAGG AGGAGGAGGG CGGGCGGGTC ACCTGGAGAG GACGTCCTTC CCTGTTTCCT 1200
GGAAAGGACC AGATACCCGA AGCTGGCCAC AAGCGGGCAT GGTGGCGGGT GTCTGTAATC 1260
CCATCTACTC GGGAGGCTGA GGCAGGAGAA GCGTTTGAAC CCGGGAGGTG GATTCACTGT 1320
CTCCTTGTCT TTGTGAATTA GCAAGGACAT TTGGTTACAA GTAATAGAAG GCCCTGGCTT 1380
AAATGCTGGG GTGGGGGAGG AAACATAATT TCTCACTCCT TCATAGTAGA GACAGATCGC 1440
CCTGTAACAA AAGACAGATT ACCAAGAGAA AAGCAAGCAA 1480
|
