| Tag | Content |
|---|
EnhancerAtlas ID | HS052-38395 | Organism | Homo sapiens | Tissue/cell | Fibroblast_foreskin | Coordinate | chr9:35366990-35368470 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr9:35368186-35368207 | TTCTGCTCCTCTCCCTCCTCC | - | 6.21 |
| | | 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 |
| GH09I035366 | chr9 | 35366985 | 35368112 |
| Enhancer Sequence | GTAAGTAATT CACTGCAAGG TTTCTGTGGA TTTTATTCAG TATCTCTTGA TGCTTTTAGC 60
TTTTCCCCTG GGAAGCAGGG GAACCAGCTT CATAAGCTGC ATCCTGGGGA AGGAAAAGGT 120
TCCACTATAG GTTGGTTGGT TCTCTGAGGC AGAGGAGAGA ACTCTGCTGA TGGATTCCTT 180
GGAGGCAGAA GAGGGAACTT TGCAGAATGG TTACCCTGGT GCAGGGGAGG GAGCTTTGGG 240
GCCTTCTCAT CCTTGCCTCT ATAATTTCTG GTCCATCTTT TCATAGTGGT GAAATACTCT 300
TTAAGTAGAA CAAAGAGGAA ATTAGAAAAA TATCTGCATT TGGAAACATT TTCTTTCCAT 360
TTCATTTGTT TTTAATTTTT GTAGGTACAT ACTAGGTGTG TCTATTTATG GGTTACATTA 420
GATATTTTGA TACAGGCATA CAGTGTGTAA TACTCACATC AGGGTAAATG GGGTATCCAT 480
CACTTCAAGC AGTTATCCTT TCTTTTTGTT ACAATCCACT TACACTCTTT TCGTTATTTT 540
AAAATGTGCA ATAAATTGTT GTTGACTGTA GTCACCCTGC TGTGCTATCA ATACTAGATC 600
TTATTCATTC TATCCATTCC ATTGTTGATG GTGTGGCTGA TTAAGTTACT CCTAGGCTTG 660
ATCCTGCTCC AGCTGTTGTG AGTCATCTAC TTATTCCATT CCACTGTAGT CAGGATATAA 720
GTAACACCCC TTTCTGAGCT CTGTATGTTC TGTCCGTGCT TCTTGTTTGG GAGTTTCAGA 780
CCTGTGTGAT TGTACCAGAG TCATTTTAAG CTGCTCAGTG TAGCCTGTAA CTGACTGTTC 840
TTAAAGAGAG AAGAGAGTTC AAGTACCTTC TCATTCCCCA CTCCTTCCCA CAAATACCAC 900
CAATTAGTTA TCTAGACCTT CCTTTTCCCT TTTTCCTACA AAGGCTTCTG ACATCAGAAG 960
TCTCAGTAGT TGCTTCCTCT TGTGGCCAGG GAAGAAGAAA GATCAGGTAG ATGATCTACT 1020
ATATTTTTAC ATGCTCCTTT CCCTTGCAAT TTGTCATCTT TAAAAAAAAA TTTTTTTTAA 1080
CTTTTGTTTT AGGTTCAGGG GTACATGTGC AGGTTTGTTA TATAGTTAAA CTCGTGTCAC 1140
AGGGATTTGT TGTACAGATT ATTTCATCAC CCAAGTACTA TAACAATAGT TATTTTTTCT 1200
GCTCCTCTCC CTCCTCCTAC CCTTCACCCT CAAGTAGGCC CGTGTCTGTT GTTACCCTCT 1260
TTGTGTCCAT GTGTTCTCAT CATTTAGCTC CCACTTATAA GAGAGAACAT GCAGTGTTTG 1320
GTTTTCTGTT CCTGCATTAG TTTGCTAAGA ATAGTGGCCT CCAGCTCCAG CCATGTTCCT 1380
GCAAAGGACA TGATCTCGTT CTTTTTTATG GCCACATAGT ATTCTGCGGT GTATATGTAT 1440
CACATTTTCT TTATCCAGTG TGCCACTGAT GGGCATTTAG 1480
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