| Tag | Content |
|---|
EnhancerAtlas ID | HS055-01388 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr11:13155940-13158290 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr11:13156527-13156548 | GGAGGAGGAGGAAGAGGGCTG | + | 6.24 | | ZNF263 | MA0528.1 | chr11:13156524-13156545 | AGAGGAGGAGGAGGAAGAGGG | + | 9.24 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 13156857 | 13157590 | | chr11 | 13157600 | 13157793 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I013134 | chr11 | 13155725 | 13158506 |
|
Enhancer Sequence | TTGACTCCTC TTATTTTCTT ACATTTCACT CAGGTAATCC CACTGGTTCT ACAGAATCCA 60
GAAATCTACC ACACGTCACC ACCTCCACTG CCACCACCTA GGTGCAAACC CCATTTTCTC 120
TCACCTGCAC ATCAGTGGCT CTAACGGGTC TGTCTGCTGT CACACTCACC CCTGCAGTGT 180
TTTCCACATA GCAACAATGT GACCCTGTTA AAAGGTGAGG CAGAGAGTGT TGCTTTTCTG 240
CTAGGAACCC TCTAATGCAG TCATACTTTG CTTAACAAGG ATACGTTCTG AGAAATGCAT 300
CATTAAGCAA TGTATACACA TTTATCCAAA CATAGAAAAG GTGCATTAAA GATACAGTAT 360
AAAAAGTTTA AAAATGGTAC ACCTGCATAG GGCACTTACT ATGAATGCAG CTTGCAGGAC 420
TGGAAGTTGT TCTGGGTGAG TCGGTGAGTG AGTGGTGAGT GAATGTGAAG GCCTAGGACA 480
TTACTGTACA CTACTGCAGA CTTTATTAAA CACTGTACAC TTAGGCCACA CAAATTTATA 540
AACATATTTT TCTTTCTGTA ATAAAAAAGT AACCTTAGCC AACCAGAGGA GGAGGAGGAA 600
GAGGGCTGTG CTGCCTGGTG TCCGCAGCTG AGAGACTGGA TTGGGGTGCC CCTTTGGGAG 660
CTCTCTGAAA TCCCCAAGGG ACACTTTGAA GGGAGCTATT TATCCATAAT CAAGGAGCTG 720
TGGTTAATGC CATCCTTATT TGGGTACTGA AAGGAAGTGT GACCTTCTTT AGCGGTTATA 780
GGCTTTTAGG GCAAGAATCA TTTATGCTAC AGTAAGTTTT GCAAAATGTT CTTGCCCAAA 840
TTCATCTTTA GGAATGAGTG GTTTGATTTT AGTGCATCAA GGTAAGCCCT TCTTTGTTTG 900
AGAGGGAAAA ATAACAAAAT TACATTTTCC TCGTAGCCAG AAGCATTTCT GACTGTGCTT 960
ACAATAACAT CATCTGATGA ATGCAAATGT GTGGGTCTGT CTTAGTTGTG CCCTTTGTAA 1020
ACTAACCAAT GGTGAAGGCT TTGTTCCAGC TGACCACATG AAATAGGAGG AGGCTTTCTC 1080
TCCCTCTCCA CTGAGTTGGA GGGCAGCCAC TCTCTATTTC CATTGGAAGA GCATGTCACC 1140
CGATATTGCA CAGACTGGGA TGAACACAAG AGGCCTTTAT CTTGGTTACT GGATCACAGT 1200
CCTGTGCAAT TTTCATTACC TGATTGGCTG CAAGAGAAGG GAAGAGTTTC CCAAGGAAGC 1260
TACAGATATG AGAGCACTCC CAGGAATTCA AAGACCTCTT AGTTAGGGGC ACTGGCCGTC 1320
CCTATTGTGA GCAAAGACCA ATGCCATTTT TTACCTAACA AAGCTCACAC TAGTGTATGG 1380
GTGCTGTGTG GGGAGTGGCA TGTGTATGTG TATGTGATAC TCCCAGGATC TATATAGTTT 1440
ATCCTCTTTT TATACTTCAA AAATATTTTG GAAAGGAACT TCTCTACAAT GTGCCTCGGG 1500
CTGCTTCCTG TTCCCATTTC CCTGCATAAA CACAGGGTTG CTTCTGTGAA TAAAACAAAA 1560
ACCACCTCAG AAAGCAAAGT CTAACAGGCA CAGGAACCTC AGTCCATGTG CCAGCTGCCT 1620
GCCTCCCATC AGGAGGGAAG GATATATACC CCATATATAT TGAGCATTTA TGGTGAACCA 1680
GACACTTTGC ATGTTACTTA CCTTAAACTT TGAGTCTTAT GATCTCTTCT ATAGGGTGCA 1740
CTACTGAGAT AGGTTATCTG AAACTGCAGA GCCCCTTCCT TAGCCCAAGC TTCCACCCAC 1800
TTCTTGCCTG GATTTTTGCA ATGGCTTTCC AGGTGATCTC CCCACTCCAA AATCTTTTCA 1860
CAAGACAGCC AAGACAAAGT TTTCAAAGTA CATGTCTGGT CAGGTGACAC ATATATACTC 1920
TTCACTCCCA CCCCCACTGC TAAAAAGCCT CTCATGTTAT CCAGTGCTTT TAGCACAAAG 1980
ACCAGATCCC CTACAGTAGC CAGAGCAGCC CTGTGTGATT TGATCCCTTC TCTGTCTTCA 2040
GCTTCATGTG GTCCTGCTTT TTCTCAACTC GCTGAGCTCC AAACACACAT TGCTGTGCCA 2100
TGCTCCTGTC TGGCACAAGA CCTTCCCATG AACTATTACT TCTGCCTGGG GAACCACGCA 2160
CAGGCCCACT TCTCTACCCC ATCCCAGCCT TCCTCAACCC TGTGCATCCT TAAGCTCACA 2220
GTTGCCATGT CACTTCCTTG TCATGCCTTG GAGTCCTGGC TATGCTACCT TTGCAGCACT 2280
TTTCACAATT TTTAATGAAC GTTTGATTAT CTTCTGACTT TCCTAGTAGA CTGGGACTTT 2340
TGTCTTTCTC 2350
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