| Tag | Content |
|---|
EnhancerAtlas ID | HS146-06264 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr17:17348760-17350180 |
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 | CCATGCTGAG CACCTTTCTG ATCCTATGTC ATTGCTGGCG TTTGCTTTTC CTCCCCTCTC 60
AGGATCCAGA TGTTATCATT CCCCAGGAGC TCAAACTACT CCATCTCCCT GGTCTCCCAT 120
CGTTGAACTC CAATCATGGA AAGAATGCCA TACAAGCTAG TGCTCCTCAG TGTACCAGCC 180
AGGACTCTGC AAGTGACAGA AAGCCCCGCA CACAGGCTCC AGCCCATCCT CAGGTCTCTG 240
CCTCCTGCTC CGGCTCTGGC TTCCTCCGCA TGTTGGATTC GTATGGGTTG GTCCCCAGCT 300
GCCCTGTGAG GCAAGGCAGG CCTTGATGTT CACTTGCCAT ATCAGGTCCC GCCTGCCTCT 360
GCAGAAAAAT TTTAGGCTCC TCAAGGTCTG GGTCCACTTC TACTCCTCCT ATCAGAGTGT 420
AAATAAAAAC AGTCTCCTCA TCCTGCCCCT GCTCATATAA CCTCTGTGAC AGGATGCTCA 480
CTACTTGGAG AAGTAACTCT TTTTGCGGAG CTGGTCTCCG CCCCTTCTGT GACTGCCACC 540
CACTGGGCCA GTTCTGCCTA ATAGCAAAGA ACACTGCTCA CCAATCTTCT TTCCTTTCCT 600
TCCTTCCCTT TTGCCCATAA GTCACCGATG GATGGACTGG ACCCATGGGC AACGTCTGTG 660
GATGACGCTG TGTTTGTCCT TCCACAGGGC GTGGGGCTCC TCCACCCTGC ATCAGGCACA 720
AGCCTGCTTT TGGGGAAAGT CCCACCATCT CATTTTCCCT TGCCTAAAAT AGCTACTTCC 780
TTTATGGGGA ATGCAGTGTG GTGGGGAGCA ATGAAAGGGA TGAGGTAAGT CATCCACAGA 840
TGCCTGGTTT GGAATCATTC CTGAAAAGGT CAGCGTTTTC ATCAGCCAAA CAGGAGGCAG 900
GGCACTTCCG GCTGGTCATT AACCAAGGCA AACAGCGTGG CGGGGAAAGT CAAAGCCATA 960
GCCAACCACA AACAAACAAG TCATGTATCC TCTGTGGAGG TGACTTTCTT CTGAAGGAAT 1020
GTGTGGTTGT TTGCAGATAA TATCAAATCC ATTTCACGTC AGATCAGGAT GACAGACAGC 1080
CAGAGGCTAT TGGGGTCTCA CATTAAATGG CTCTTTTATG GTAATAAATT GTTTCCTTTT 1140
CACGGTTGCA TGAGCAATCT CAAGTTTTAT TTTGAGGTGT CAACTGCCCT CAGGGACACC 1200
TGCCACAGGT GGGATCTTGG GTCCTGGCCA CCATATGTGA GAGAGCAGAC CCTGGCTGAG 1260
TCACTCAGCT GTGGTCGCAT CACCTCTGTC CCTGCCCCAC TGCTCAGCCC CATGCAGGCT 1320
GGCAGGGGAG GCCTCCTCTC CCCCATGGGG TCTCCCTTTC TTCCTCTCAC ACTGATCATT 1380
GGAAAGAGTG GCTTGCATTT GCCACAGTGC TGAGGGCTGT 1420
|
