| Tag | Content |
|---|
EnhancerAtlas ID | HS038-02716 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr10:80783900-80786420 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr10:80786392-80786404 | TGCAGTGATTTG | - | 7.22 | | RREB1 | MA0073.1 | chr10:80785423-80785443 | CACCACACCACCCCCTCACA | + | 7.13 | | ZNF740 | MA0753.2 | chr10:80785177-80785190 | GTTGGGGGGGCGG | - | 6.27 |
|
| | 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 |
| GH10I079022 | chr10 | 80782057 | 80785900 |
|
Enhancer Sequence | TATGGACATC ACAGAATCCA AGCCCCTGAA ATAGCCACCT CTTCTACTGT CTGATAACTG 60
AGCAGCTCCA GCTTCAAACA CTTCACACTC AAACAGTGGG GCATCCATGC CAGAAAAAGC 120
CTGGCTGGCC TGCAAAGGAA GAAAGATGGG GCCACTGGCC TTGCAGAGCC TCCCGTCCCA 180
GACAGGGTAG AGTGTGGAGA AGAGGTGGCA GCCGCGCTCA GAGCTCCAAG AGAGCCCCCT 240
GGGCAGGAGC TAGGTGGGCA AGCAGAAAGG TGGGGAGGCC CTGCCTATAG AAGCAGCAGC 300
CTGAGTGAGC GCTGGGAGCC TGCAGAAGAA GAGGTTGGAG CCCAGCAGTC TGGGCAAGGA 360
TGAGGCCAGG TCTGGTGTGG GGACCCTTTA TACCCTCTCT TCCCACCCTG TACTTCTCAG 420
TCCCAGCTGG AAGCATGATG TATCTCCCCA GCTAGATGCG AGGCTCCCTG AAGGCAGGCC 480
TGGGGGGCTC ACTGCTGAAT TCAGAGCCTG GCCCAGAACA AGTGCTCAGT AACTATGCGG 540
AGTGAGTGAC AACAGATACA GGCTAGGAGG GCCTGGGATA ACTCTGAAAA CAGAGCTTCT 600
GTGCAACAGC AGGCTTAGCC CTTGTTTCCT GATAGATTTT GGCTGTTGCC ACCAAGTGGG 660
AAAGGGAGTG GTGGGGGAGG GGACCTGGAG AAGGGGAGTG ACCTGACAGC AGAGGTGTCA 720
GCAAGGCCCA GGAAGGGGTC AGGGCCCCAT CCTGCAGGAG CAGCTCTGCC GGCAGCTGGG 780
TCAGGCTCCC AGGTCCAGAG ACGCCCCATG CTCCACTGTA GGGATGAGGC CACAAGGCTG 840
GTCTTTGCCC CCTACTAGAG TCTGAGGCTC CAGCAGCTGA TCTGGGCCAG CTCGGCAGAG 900
AGCTGGATCT GGGAATAGGC TTTCCTCACT AGGCTACAGG AAGGAGCGAT GCTGCTGAGG 960
CCTGATGTTC ATGCAGGGAG AAGGCTGGGG TACCAGTGAT GCCCAAGGAC AGCTCCTCTT 1020
ACACCCATCC CTGGTCCAGC TCCCTCGTTG TCCTTAGCAA GTGGGGGACC AACTGAAGTC 1080
TCTGAAGTCT GCAAGGTGGG GCCGTCAGCT GAGGCCCACA ATGACGTCTG TACTCCCCCA 1140
GTCACAAACA GGCATGCACA CACCCACAGG CACACACTGA CACACACATG CCCAGCGTGG 1200
GCTCTGTGCA GGCGGGGTCC TGCTGCAGGA AGGGCTGGTG CGGCTGCCAG GCAGCAGGCC 1260
CAGCACAAAG GCACAGGGTT GGGGGGGCGG TGTTGGCGGC ACAGGAGTGG GGGAGGGCTG 1320
CGAGGGATGT GGCTCAGAGC CTAACAGGCC ACCAGCAGCC GTGGCATCTG CTTTTTCTCA 1380
CCTCTAAAGG GAATCGATTT GTCTCTGACT GATTTCCCTG ACGTCTAGTT TTCTTCTCCG 1440
CCCGGCTGTC AGCCCAGCCA CTGCACACAG GGAAGTGCGG GGGGAGCACC TTGACCGCCT 1500
GCCTGCCAGC CTCTCTGCCG CCTCACCACA CCACCCCCTC ACACACACAA CACACGCTGC 1560
ACTCACACTC ACACGCCCGA CAGAGAAACC CACACCCCAC ACCCGCACCA CAGCCTCCCG 1620
TCCAGACACC CACACTCCCA CCTGACAGAC AAACCTGCCA TACACCGTAC AGACATATGT 1680
AGACAGATGC ATATGCAAGC ATGCACACAC ACACAGTACA AACACAGAGA CAGACCTGCC 1740
ACACGCGATA CAGACACATA GTTTTACTGT GTGTAACATA GGTATACAGA CACTCTCACA 1800
CACGCACCAC AGTACAAACA CACACACACA CAAACACACA CTCCCACTCC ACAGACAGAC 1860
CTGCCACACA CCACACAGTA TAAACACATA CACAGACACA TGCAGACACA TCACACACAG 1920
AAAGATGGAC ACACACACAC ATAGACCCAC ACACAAAGCC TCCACACTGA CATCCCCAAG 1980
TACCCCAGAG TCACCACCAT AACCCAGACA CACACACACA CACACACACA CACACACTAC 2040
ATTACCACTC TCAGATACCA AAAGGGACAC TGGCACACAC AAGCCTCACA CTCTCAGATG 2100
GCCCCAACAC TCACGCACCC CACACATTCA CACAGCCACA CAGGCTGCAT CCCTGCTCAC 2160
ACAGCTACAC ACACCACACA CACACTCATA CTCCCTGATC CCCACCAACA CCCCCCTCGA 2220
CACGAGCACC CACAGTCATG CACACCCACA CAGTCCCAGG CCACATGGGC ACTCCTCGCT 2280
GTCCCCGCCC ACCCCAGCAA CCCCTACTTC ATCGTGGAGC TGCTCCTGGC CCCCCGAGAG 2340
TAGTAACGGC CCCCTTGGTG GAGGCAGACA TAGGTGTGAC CCAAAGAGGT GGGCAGGGCC 2400
TGGCTGGGGG GCACGGGGGA CCCCAGGGTG CTGCTCATCT GGACAGGCTC GTTGCAGGGC 2460
AGCCTGGGTG AGGAGCTGGA CCCTGGCAGG GCTGCAGTGA TTTGGGGCAG GGGTGGGGGT 2520
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