| Tag | Content |
|---|
EnhancerAtlas ID | HS052-27174 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr3:136732320-136733790 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:136732899-136732918 | TGGCGCCACCTTGTGGTCA | - | 8.07 |
| | | 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 |
| GH03I137013 | chr3 | 136732321 | 136733734 |
| Enhancer Sequence | GGCCAAAGTT GGGACAATAT AAGCACCAGA AGGAGAATAT TGGCTGGCAC AATTGATACC 60
ATATATTTGA AAAGTCATCA GTCCATGACA CCCAAGAAGA GCGAAGCTAC CATAATGCAT 120
TCTCAGAGAA GATGAATCTA ATAGAATGCA TTTCTACTTG TTATTCAATC GTGTTGGGCT 180
TATCGACTCG TTTATCGTGT CAATGAGGAA TACCAGTAAA TGTAAATCCA TCAGTCAGAA 240
GGCATTTTTT CTCCTCTAAA GGCTCCTCTC CGCCCCTTAA CGTCCAGTCT TTCCCCACTT 300
GGCTCTCCCT GTCCTGTCAA GGGGTTCGGT GGAAAAGTCT TTTAAGTTCC CTTCACAGAA 360
GAATTGTAGA CTCTGCCGGT CTAGTCTCTG GGCCAACCCT CCCCGTCTCT TTAGTAAAGA 420
TGTTTTTTAT TATTTTCCTT GTGCCGTGTA TTATCCTTAG GCTAGAGTAA CTTTCCGGGC 480
CTGCAGACCT CTTGGTTTCC TTTCAATCTG GAGGACTTGA TCCCATGGCC AGCTTCGGAG 540
CTCACCAGGA GGGGAAGACC CATTACATCC ACGGGCGTCT GGCGCCACCT TGTGGTCAGT 600
GCTGAAAATG TTTTCTGTTC CCACTCGCAA TGAAACTCCC TGGGCTTCCT GGATGAAGAA 660
AGGAAAGCTC AGGTCGGTTT CCTAGAATAA TAACTCAGTT ACACAGTTTC CACGGGCTTG 720
GTCCTTAACA AACCTCCACT GTCACTGGTG GAGTTAGAAT TTAGCAGCCA CCTTCTCCTC 780
GCTCTGTGTC TGTATCTGTC CCGAGCTCAT GGTTTGGGGC TTCACGCTGT ACCCACGGCT 840
CTCGCTCTTT TCTGGGACCT TGGCCTCTCG CACTCTCCTG TCTGTTGATC TTTCCACCAT 900
GCTGCCATTC CCTACCTCTC GGAAATAGAC TTTTTTTGGA TGTCTTTTTG TTTTCCTTCT 960
GTGTGACCTA TTTGTAGGAT CCCTTTACTA GACTGACTTT CCAGGAGTGT TCCTCAGCCC 1020
CCGCACAGAT CAGTAGGGAG GAGCCTGCCT GCTGCTTGCT CATGCTAAAC CAGCGTGCTG 1080
CCCAGCCTGT GAAGTTTGGA ACTGGAACAC TAGAGTTGGC CCCAAATTAC AGCTTTCTCT 1140
TCTGGCTCCT GGGACTCCCA GTTTCTTCAG CAACAACAAC AAAACCTGGA AAAACGTATC 1200
CTTGCCAGAG GTGGGAGAAT GAGGCTCACA AAAGGAAAAC ACGGACCTTT CTTGTCTCCC 1260
CCAGTGAGAG GTTGCAAGAT CAGGTTGTAA AACCCCATTA AGGAGGACCT TAGAGGAAGA 1320
ACTGAGCAAG GAGCCTTCTC AGGTGCCTGC AAACATCTCC AAGAGCAAAA GTATAAATCC 1380
TCATATTGTG GAGGAGGTAC ATGTTCCTGG TTCCTTCACT GGACCTCACT GAGAAAATTA 1440
AACAAACAAC AACAACAACA ACTACGTTAA 1470
|
| |
|
|
|
