| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13114 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:17349120-17350470 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr17:17349661-17349672 | GCACTTCCGGC | + | 6.14 | | EWSR1-FLI1 | MA0149.1 | chr17:17349357-17349375 | CCTTCCTTCCCTTTTGCC | - | 6.03 | | EWSR1-FLI1 | MA0149.1 | chr17:17349353-17349371 | CTTTCCTTCCTTCCCTTT | - | 6.23 | | EWSR1-FLI1 | MA0149.1 | chr17:17349349-17349367 | TTTCCTTTCCTTCCTTCC | - | 6.2 | | ZBTB7A | MA0750.2 | chr17:17349660-17349673 | GGCACTTCCGGCT | - | 6.48 |
|
| | 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 |
| GH17I017444 | chr17 | 17347707 | 17350904 |
|
Enhancer Sequence | GCAGAAAAAT TTTAGGCTCC TCAAGGTCTG GGTCCACTTC TACTCCTCCT ATCAGAGTGT 60
AAATAAAAAC AGTCTCCTCA TCCTGCCCCT GCTCATATAA CCTCTGTGAC AGGATGCTCA 120
CTACTTGGAG AAGTAACTCT TTTTGCGGAG CTGGTCTCCG CCCCTTCTGT GACTGCCACC 180
CACTGGGCCA GTTCTGCCTA ATAGCAAAGA ACACTGCTCA CCAATCTTCT TTCCTTTCCT 240
TCCTTCCCTT TTGCCCATAA GTCACCGATG GATGGACTGG ACCCATGGGC AACGTCTGTG 300
GATGACGCTG TGTTTGTCCT TCCACAGGGC GTGGGGCTCC TCCACCCTGC ATCAGGCACA 360
AGCCTGCTTT TGGGGAAAGT CCCACCATCT CATTTTCCCT TGCCTAAAAT AGCTACTTCC 420
TTTATGGGGA ATGCAGTGTG GTGGGGAGCA ATGAAAGGGA TGAGGTAAGT CATCCACAGA 480
TGCCTGGTTT GGAATCATTC CTGAAAAGGT CAGCGTTTTC ATCAGCCAAA CAGGAGGCAG 540
GGCACTTCCG GCTGGTCATT AACCAAGGCA AACAGCGTGG CGGGGAAAGT CAAAGCCATA 600
GCCAACCACA AACAAACAAG TCATGTATCC TCTGTGGAGG TGACTTTCTT CTGAAGGAAT 660
GTGTGGTTGT TTGCAGATAA TATCAAATCC ATTTCACGTC AGATCAGGAT GACAGACAGC 720
CAGAGGCTAT TGGGGTCTCA CATTAAATGG CTCTTTTATG GTAATAAATT GTTTCCTTTT 780
CACGGTTGCA TGAGCAATCT CAAGTTTTAT TTTGAGGTGT CAACTGCCCT CAGGGACACC 840
TGCCACAGGT GGGATCTTGG GTCCTGGCCA CCATATGTGA GAGAGCAGAC CCTGGCTGAG 900
TCACTCAGCT GTGGTCGCAT CACCTCTGTC CCTGCCCCAC TGCTCAGCCC CATGCAGGCT 960
GGCAGGGGAG GCCTCCTCTC CCCCATGGGG TCTCCCTTTC TTCCTCTCAC ACTGATCATT 1020
GGAAAGAGTG GCTTGCATTT GCCACAGTGC TGAGGGCTGT CAGTCTTCAC AGCTGAGGAA 1080
ATGACATGAT TTGTTGGGAG CCACTTGAAA TAACCAGTTC CCCAGCTGGT CTCGCTGTCC 1140
CTGTGCTGGC AGCCCTGCTG ACGTGGGGCC TGGCTAGACA GAGGTGGGCC TTCTGTGCCC 1200
TCACCTGGGC CATCCCCACC ATGCGGTGAG GTTGGGTTGC ATCCAGCCAG GAGGCAGCTG 1260
GCAGGGCCCT GTGGCTTGTC TGAGGACCCA AGGGGGAACT TATCAGAGGG CAAGAGAGAA 1320
AGAGGGCTGA GGGGTGGTAT GTAAGAGGGA 1350
|
