| Tag | Content |
|---|
EnhancerAtlas ID | HS052-06118 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr11:9158890-9160370 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr11:9158902-9158919 | TGCTTTATAGTAATTCC | + | 6.74 | | EWSR1-FLI1 | MA0149.1 | chr11:9159368-9159386 | ACTGCCTACCTTCCTTCC | - | 7.25 | | Gfi1b | MA0483.1 | chr11:9158958-9158969 | AAATCACAGCC | + | 6.02 | | TFAP4 | MA0691.1 | chr11:9159219-9159229 | ATCAGCTGTT | - | 6.02 | | Zfx | MA0146.2 | chr11:9159278-9159292 | CAGGCCTAGGCCCA | - | 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 |
| GH11I009136 | chr11 | 9158444 | 9162278 |
|
Enhancer Sequence | TATAAGGGTG CTTGCTTTAT AGTAATTCCC TGAGTTCCTT TGCTTGCTTG TTTATTTACC 60
AGTCCCTGAA ATCACAGCCT GGGAAGCCCT GAAGTAGAGC AGGTGCAGAA GCTGAGGCAG 120
GCAGGGCTGC TTGCTGAGTG AACCAAACAC ACCTGATTTA CCCAGGACCA CTGGAGAGGC 180
CTGGCTGGGC CCTACACGGA AGAACGCAGT TGACTCAAAT GTCCTTGAAA TCTTGAGCTA 240
CTAAACAGGT CTGTTCTCTT ATATCACACA TCATTCCAAA ACAGATTTGC AGAAGATTAC 300
AAAACAAAAC ACAGTAGAAA GTGAGTAGGA TCAGCTGTTA CAAAGAGCAA GGAAATAGTT 360
GGTCCCAGCA CCTGCCTTAA GGTAAGCTCA GGCCTAGGCC CACAATATAA ACACATACAG 420
CTGAGTTCCA TGCTGCCCTT CTTGCCCAGC CAAGAATCCC ACTTCCTGCT CCAGAGGTAC 480
TGCCTACCTT CCTTCCCCTT TCCTCGGCCT TCTCCGAGAG AACTAAAGCT CTGTCCGTGG 540
GCTCCAGGCA GACGGCTGCA GTGTGGCCTC TCACCCCCTC TGCAGGCAGG ACGCTGCGCT 600
GCAGCTCTCT GGGCCCTCTC CTCATCTCTT CAGAAGCATT TACCACCTGC CAGGCCCAGG 660
GGATGGAGAC AGGCAAGAGA TCCCCCTTTT CCCTCTGGGA GCTCACGGTG CAAGGGCTGA 720
GCCTGACACG AAAGCAGGCA ATGACAATCC AGAGAGGAGA TGCCAGCATC TAAGAAAATG 780
AAGGAGCACA AGGATGGAAT GATTAACTGC CTAGGGAGAT TGGGGACACT TCACAGCAGG 840
TGACTGCTAA AGTAAACCCT GTACAACAAA CACAAAGTGG GTGAAGGGGA GGCATTCCAG 900
GCAAAGGGAA AATGCATGCA AACCAGGAAA GCATAAAAGA GGGCACTGAT TGGTCTGAGG 960
TGCCTGACTT GATCACGTTA CACTTCTTCT GGAGCTTCCT GCCAAAGCAG CCTGAAGAAT 1020
AAAAATGAAC GAAGCTGGAC CTCTCATAAA GGTCTCCCAC CTGCCATCCC CAGGAAAGCA 1080
AACCTTTCTT TCAAGAGCTT CCCCCGACCC CCAGCTTCCC ACACCTGGTC TCCCTTACCC 1140
TCTCAAGAAA GGGCCCATCC TGTCTCAGTC AAGTGACAAC CTCTGCACCC CTGGCCGGGT 1200
CTTTTCCCTC CTGTGTCTCA GTCTCCTCCT CTGTGGAGTG GGGAAAGAAC CCTGTCTGCA 1260
TCCATGTGAA TCAGCCACAT AACAGCTAGG AAGGCTCCTA GCACTGCGGG CAGAAGGACC 1320
CAGGAGACCC CAGGCCCTCA GGGGCATCCT GGGCAGGCCA CAACCCCGAG CCTGCTGGTA 1380
AAGAGAGGTG ATGCCACAAG ACCATCCTCA CAGATGGACC CAACTGCACC CGCAGCCACC 1440
CACTGCTCAT AAACCTCCAT AAAAATCAGT GATCCATGCA 1480
|
