| Tag | Content |
|---|
EnhancerAtlas ID | HS062-03570 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr12:12480280-12481430 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr12:12480921-12480940 | TACTGCCCTCTAGTGCTCA | - | 6.32 | | ZNF263 | MA0528.1 | chr12:12480829-12480850 | TGAGGAGGAAGGAAGAGGTGA | + | 6.02 | | ZNF263 | MA0528.1 | chr12:12480824-12480845 | GGAGGTGAGGAGGAAGGAAGA | + | 6.11 | | ZNF263 | MA0528.1 | chr12:12480817-12480838 | AGGGGAAGGAGGTGAGGAGGA | + | 6.32 | | ZNF263 | MA0528.1 | chr12:12480821-12480842 | GAAGGAGGTGAGGAGGAAGGA | + | 6.46 | | ZNF263 | MA0528.1 | chr12:12480832-12480853 | GGAGGAAGGAAGAGGTGAGGA | + | 6.61 | | ZNF263 | MA0528.1 | chr12:12480847-12480868 | TGAGGAGGAAGGAGAAGAAAA | + | 7.35 |
|
| | 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 |
| GH12I012327 | chr12 | 12480327 | 12481490 |
|
Enhancer Sequence | CCACCATCCT AGGGGCAGTA AGTAGAGAGA GCTGTGTGAG AAGAGCACTC TTTCCACTCC 60
AGATGTCCCC TACAACCTAT ATCCTCACGG CCACTAACAG TTTGGGCCCG TAGCATCACT 120
CATCTGGACC GCTCCCATGT GGTCTCCCCA TCACAACAAA GACTGCAGCA AGGTGGACAG 180
AGAACTCCAA GAGAGCCAGG AAAATACCTT TATAAACCAT CACAGAAAGC CTGATTTCCA 240
CTCGCTAAAT CCATTAATAA AGAGAGGAGA AATTTTAAAA TTCCAAGGCA CCTGGTTACT 300
AATCTGATTC TGGCCTACAT GTGGATATTC AATAAATACT TGTTAAGTTA AATTGACTCA 360
AGGTTTTATT TATTCAGCCT ACTTAAAGCT TATGTAAACC CCTTGGAGAT TTGTGTCAAG 420
CTGTTAAGTT GGAAAATATA AGAAAAGTAG TATTTTCAAT AGACCAGCTT TCCTCTTAAT 480
GTACTTTATG AACTTAGTGT AAACCAGGGA AATGGGGGAG GGGTACCAGA AGAGCAGAGG 540
GGAAGGAGGT GAGGAGGAAG GAAGAGGTGA GGAGGAAGGA GAAGAAAAGC CTTTTCTGTC 600
ATTTCCTGCA TTTGTCTTAA TTGCTGTACT TATTAACCAG CTACTGCCCT CTAGTGCTCA 660
CTGTATTAAG TTCGCATCTG AATTCCATTT TTATCTTTAA AAACTCTGGT GACACTTGGA 720
AGGGATCAAA TTTCCTGTTT TGCAGATAAG CAAATTGAAG TCCAGAGGAA AGAGGTATCA 780
AACTGACCCA GGGGACTTCT GGACTCTTTG TTACCTCACC TATAACTTGT CTGGAAAACT 840
TTATTAAAAG CCTTTCTCAG AAATTTTAAT TGGTAACCAG TAAAAATTGT AGCATCATGT 900
TAGTGCTAGT TATTATTATT ATTATTTTTG AGACGGAGTC TGGCTCTGTT GCCCAGGCTG 960
GAGCGCAATG GTGCAATCTG GCTCACCGCA ACCTCCGCCT CCTGGATTCA AACTACTCTC 1020
CTGCCTCAGC CTCCCAAGTA GCTGGAACTA CAGGCGCCCG CCACCACGCC CGGCTAATTT 1080
TTTGTATTTT TAGTAGAGGC GGGGTTTCAC CGTGTTAGCC AGGATGGTCT CGATCTCCTG 1140
ACCTCGTGAT 1150
|
