Tag | Content |
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EnhancerAtlas ID | HS112-09492 |
Organism | Homo sapiens |
Tissue/cell | KELLY |
Coordinate | chr3:14954110-14956500 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr3:14955850-14955869 | GGCTGCCCCCTGGTGGCTT | - | 6.93 | RFX5 | MA0510.2 | chr3:14956030-14956046 | AGTTGCCATGGCAGCA | + | 6.02 | RFX5 | MA0510.2 | chr3:14956030-14956046 | AGTTGCCATGGCAGCA | - | 6.12 | ZNF263 | MA0528.1 | chr3:14955436-14955457 | TCTTCTTCCCCACACTCCCCC | - | 6.3 | ZNF263 | MA0528.1 | chr3:14955398-14955419 | CGTTTCCCCTCTCCCTCCTCC | - | 7.06 | ZNF263 | MA0528.1 | chr3:14955404-14955425 | CCCTCTCCCTCCTCCTCCTCT | - | 8.84 | ZNF263 | MA0528.1 | chr3:14955401-14955422 | TTCCCCTCTCCCTCCTCCTCC | - | 9.83 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_25472 | chr3:14954424-14956503 | DND41 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I014912 | chr3 | 14954425 | 14956503 |
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Enhancer Sequence | TTCATTCTGC AGCTTATTAT CCATCTCCTC TGCATGCCAG GAACTGTGCT GGTGTGTAGA 60 CATGGCCTTT GCCCTGCTGT GGGTCTTGGA GTCCAATAGT GGAAGACATT TTTTATTCCA 120 TGTTAGACAA GTCTAAATTT TAGAAATTCT TGGCCAGGCA CGGTGGCTCT TGCCTGTAAT 180 TGCAGCACTT TGGGAGGCCG AGGCAGGCGG GTCACAAGGT CTGGAGTTCA AGACCAGCCT 240 GGTGAACATG GTGAAACCCC ATCTCTACTA AAAATACAAA AAATGAGCCA GGCATGGTGG 300 CGTGTCCCTG TAGTCCTAGC TACTCAGGAG GCAGAGGCAG GAGAATTGCT TGAACCCAGG 360 AGGTGGGGGT TGCAGTGAGC TCAGATTGCG CCATTACACT CCAGCCTGGG CGACAGAGTG 420 AGATTCCATC TCAAAAAAAA AAAAAATTCT CTCCATTGAG AGAAATCCCC AAATGTAGGG 480 GCAGGTAATG AGCCAGACAG AGCTGGTTAG ATCCTGCTCC ATGGTACACT TACTACTTCT 540 GTGACCCTTA GACAACTCAC AGACATGTGC GAGCCTCAAG TCTCCCCCCA GGAAAGTGGA 600 AAGACTGGGT GGTTTTGAGA ATTAAATTCC TGGCATTTAA TTACATGCCT GGCAGGTAGA 660 AGCCGCTTAT CTGATAGTAG TTGTAACAGT TTCTCCCTTC CCGCTGACAG TTGTTCCATG 720 GGACACAGGT CCTCCCTCTC TATCTAGAGC TATAGATCTC ATCAGCTCCC TGCCCCAGCA 780 CAGCCCTGCA GGGAGTTGGG TCCCCGTGAA TTCCCCCTCT TCAGGACGCA AAAGGGAGGC 840 CATACCGGAT GGCAATGGGG AGGCAGACAG ACCAGATGCA GACCCCAGAT GCAGACCCCA 900 GCTCTGACAG CTACTGGTGT GAGACCCATG AGCACATCCC ATTACCTCCC CGAGCCTCAG 960 CTCCCTGATC TTTAAAACAA GGGAAGCAGT GAGGCGGCAG ATGGCACAGG GCAGAGCTCT 1020 GTCTTGGCCC CTCAGCCATT TGCATCTGGC CACCTCCTCT GGCCATGCCC CTCTGATCTC 1080 TGCACCTCTC CCAGGGACCT TGAATGCCAG GAACAGACAC AACAGCCTGG CTTTCCCCAA 1140 TCTGTCCTCA CCTCGTCCTC CACTTCATCT GTCCCTGGTC TTGGCTCACT GGCCCTCACA 1200 CACCTGAAGC TCTTTGAGAA GGGTGCCAGC TCCTCCCCTT CAAGCCAAGC TCAGATAGCA 1260 CCTTCTATGG AAGCCTAGCC ACCACCCCCG TTTCCCCTCT CCCTCCTCCT CCTCTAGCCC 1320 TGCTTCTCTT CTTCCCCACA CTCCCCCCGT CTGGCATGGC CCTTTATCAG AACATCTCCT 1380 TCCCTCAGGG ATAGGCCTGC ATCCCTCTGA TTACCCTGCT GTGATTAGGC CATCAGCCCC 1440 ACAGTCTGAA GCTGGGTCCT CTTCTTCCTC TGGCTCAGCG CAGCCCTTCC ACTGAGCAGT 1500 GTTGATAACT CTCTAATGGA GGGATACATG GGAGGAGGGC GGCCCGACAG GTGCTCAAGC 1560 CAGGGAGTGC CATGGTGAAC AAACACACTT AGGAAGAATT TTTCTTCCTC AAAGGTGCCA 1620 GTTTCAGAAA ATAATCTGAA CTGCAGAACA GAGTTGGGGC ATCTGGGCGC CCACGCCCAG 1680 CAGTGTTGTT AGACTGCGGA AAGTGTCTAC CAGGCAGCGA CGTCCTTGAG CTGCAGGTGG 1740 GGCTGCCCCC TGGTGGCTTC TTACAGTGGG AAGCCCCCCT ACCCATTCAT GATGGGCTCT 1800 TCCTCCTTCC TCCAAGCTGG GGCTGTAAAG CATATACTTT GAAGCAGGCA GGAGAGCCAT 1860 GGGCAAATTA GGACGTAGCC TGGTCCCGAA AGGCGAAGGA GACCTCGGGG TGCTCATGGC 1920 AGTTGCCATG GCAGCAGGAA CTTGAGGGGC CATCACAGAG AGGCTGGGGC TGCTCTCCCT 1980 AGTGACATAG GTCAGTTCCC TGGGTCTGGG AGGGTTCATG GGCAAGGTTC ATGAACCTGT 2040 GCACAGGTTC ACTGTGAGAG CAGCCCTGAC ATTCCCTCCC GAGCACACTG GAGGGACACT 2100 CATCAAGCCA TACCCCTGGC TCCACTACCT GCTAGCTGTG ACCTCAGGCA TGGCCTCTGG 2160 CCTCTCTGGG CCTCAGTTTC TCCCTCTTGG CAATGAGGAT GATGATCATG GTGCCTGTGC 2220 GTTAGGACTG TGGGAGTGCA CGTTAGGACT GTGGGAGTGA AGTCAGGGTT TTGGTCCAGC 2280 GCCTGGTGCA GAATCGGTGT CAATGCACTG TAGTGCCTGT CACTCTTAGA AGGCAGGGCA 2340 AGAACAGGGC TTCACAAACT AGAGCTGCAG GCCAAAGCCA GCCAGACACC 2390
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