| Tag | Content |
|---|
EnhancerAtlas ID | HS095-27465 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr7:6881600-6883120 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr7:6881891-6881912 | GGGGGATGGGGGAGAGGATAA | + | 6.16 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr7 | 6881879 | 6882028 | | chr7 | 6882109 | 6882273 | | chr7 | 6882495 | 6882633 |
| Enhancer Sequence | ATATTAGTCC CAACGTCACA GAAGGAGTAC ACTACCCCTG TGATATTGTC CCTAACTTCC 60
AGAGGGGAGA GGATGAGATC ACTCCCAATA TCTCAGAAGT TGTACATCCC CCGTGATATT 120
GTTCATCATA TCCAGGGAGG CACAGGATGA CATTCCATTG AATTTCATGA CAGGCATACA 180
CGCACAGTGT GATATTGTTC CTAATACCCA AGAAGGCAGA GGATGACATT AATCCCAATA 240
AAGCAGTGTG TGTACATTAC CCCTGTGTTA TTGCCTCTAA TATCCGGGAC CGGGGGATGG 300
GGGAGAGGAT AACATTCCCT CAAATGTAGC AGGTGGTTTG ATGCCCCTCG TGGTGTTGTT 360
TTACATATCC AGTGGGGAAG ACAATAATAT TATTTTTGAT AGTCCGATTC ATCCTCTCCA 420
CCTTTCTGGA ACTCTGAGGC CGGGAGGCGG CATGCACTTT CCGTGTGATC CCCAATACCT 480
TTGCCGTCTT CTGTAGCAAG TCAGCCACAA CCGCAGGCCC GTTATCTGAG CCAATCCGGA 540
AGGGCTGTCC CAATCTACGA ATCAGATCTC GAAGAAGCAC ATGGGTTACT TCACGAGCTT 600
TCTCAGTTCG TGTTAGATAA GCCTCCACCC ACCCAGAGTA GGTACGCCCA AGAACTAGTG 660
AATACTTGTT ACCTCCACAC TTTGGCATCT CTGTGAAGTC TACCTGGAGA TCTTCAAAGG 720
GGGCTGCTCC ATAAGCTTGT ATGCCGGGTG GAACAGCTGG ACCTGGCCTC GCATCATGCT 780
GTCGGCAGCT GACACATCGC TGCCTCACCG TTTTGGCAAG GGCTGACAAA GGCGAGATGG 840
AGAAATACCA GCCTAACAAC TTTTTGCAGT GACTCCTGAC CTAGATGGGT GGTTTCTTGC 900
ACAGCCAGTA CAACTGCAGC TCCTGGCAGC TGTGGCACAG CTACTCTCCC ATCCGGTAAC 960
CAAATCCATC CTTCCTCCAT CACTTGTCCT TCCCTCTACC TGGACAAAGT CCTTTTCTCC 1020
TTTAGAATAA GCAGGTCCAA GATCAGGTGC TTGAGGGAGC AGAGGAGCTG TGACTGATGC 1080
CTGGAAAGGG GCAGATGCTG CTTTTCGAGC CTCTGAGTCA GCGCGGGAAT TCCCCAAGCC 1140
CACCAAGGTG GAAGCTCGCT GGTGCCCCCT GCAATGCATA ACTGCCACCT TGTGGGGTTT 1200
CCATACTGCT TCTAATACAT GGAAGATTTC TGGTTGATAT TTTCTGCCTT TTCCCCCAGA 1260
GTTCAATAGG CCCTTTTCTT TCTAGCATGC TCCATGCACT TAAAGGGTTA AAAAGGCATA 1320
CCGAGAATCA GTGTAAATGT TGACAGTCTC ACCCTCACTG AGCTCTAAGG CCCGAATGAA 1380
AGCAATGAGT TCAGCTTTCT GGGCTGAAGT GGCCTGGGGC AATGATCTGG CTTCAACAAC 1440
AGTGTCCAGG GTTACCACTG CATACCCTGC ACCTCTCTTT CCTTGGGTGT TGACCAAGCT 1500
GCTCCCATGC ACGTATAGTT 1520
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