Tag | Content |
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EnhancerAtlas ID | HS038-05020 |
Organism | Homo sapiens |
Tissue/cell | ESC_neuron |
Coordinate | chr12:92933690-92935070 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr12:92934263-92934274 | AGCCACTCAAG | + | 6.62 | SOX10 | MA0442.2 | chr12:92933995-92934006 | AAAACAAAGAA | + | 6.62 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_20705 | chr12:92932322-92936513 | CD56 | SE_29287 | chr12:92932455-92936223 | Fetal_Intestine_Large | SE_32511 | chr12:92931078-92935836 | GM12878 | SE_43617 | chr12:92930346-92939137 | MM1S | SE_61802 | chr12:92927333-92988757 | Toledo | SE_62925 | chr12:92932227-92990275 | Tonsil |
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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 |
GH12I092537 | chr12 | 92931121 | 92942737 |
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Enhancer Sequence | ACTCACGTAA ACTGCTGATC TCCAGGCCTG ATACACAGCA AAATGCCTAG TACTTGCTAA 60 TTGTTATTGC GTCAAGTTTC CCCAGATTGA ACCTTAGGTC TGGTCAGTTT CTCCTGGACA 120 GCAGTCATTT TGACAGCTTA GGATCTTTAG GTGCCCACAT ACCTTCAGAA CCTCAACCCA 180 TTCTTGGGAG CACTGTCTGA CCACCCTCTG AGGACCAGAA GCAGGAAGAG AGATCAGATG 240 GTGAGAGGAT AAGGACTGTT GATACCCAAG GGAGGTTGTA AAACCACTTG GGCACACCCA 300 AGTTCAAAAC AAAGAAGCCA TCACACGAGG GTGAGAGAAG AGGTATTTAC TCAGTGAGGC 360 CCCTTCCAAC CCTCATGGTA AAAGTCTACA CTTGTTTAGA AAAGAGTATG TCTGTTTTAT 420 GATTTTATTT TTTAAAAAGG GAAACTCAAC AACAAAAATG ATGATGAAAA TGACAATCTG 480 ACTATGGAAA ACAGGCTCCT GCTATTCTCA TCAGACCATC TGACAAACTA CCCAAGGGAG 540 TTTCCGAGGC CTCCCAAACA GTAACAGCAG AGCAGCCACT CAAGAGGATG CCCCGGGGAG 600 CCGCCAAACT GCAATTGCCC TGGAAATCAG ATTCGAACAG CTCAGACATG AGGGCAAAGG 660 GCGGGATGCA TGCATCCCTA AGCACCAGCC CTTCAGCCCA GCAGAGGGGC ACAGACAAAG 720 CTGCCCCGGA AGAATTGTTT GGGAGGTGCA GATACAAAGA ATAAGATCCT GCTGGCAGCG 780 CTGGGAAACA CAGCAGCAGT CGGCACACGC TGGCCCTGGC AGTCAGCAAC CGCCTGGCTC 840 AGGCTGAGCA AAACCTTTCT GTGAATATGG CGTGAAAGCA GATCTCTCAG AGGCTCATGC 900 TCCCTGAAGG TGAAAGATCA ACAACAAAAA AGGCATTAAC CCCTCTCCTA AATGATATTT 960 CATGGCCATC AAAATCCCAT CAAAGGAGCA GCTCATGTTC ATAAGCCTGG GGGAGATGCT 1020 CCCAGCAATT TAGACACATT GGCAGCCCCA GGGAGGAGGA CATAGCCTAT GGGGACTCTC 1080 TATGTGTGAA GGGCAGCAGT TTGCATAACA AATGTTCCAT GCACAATCTT GGAACATTGG 1140 CATAATTCTT TCTGGACCCA ATAATGATAA TTACTCTCTG TCCTAATTAA GGAGAAAATA 1200 AAGAAGCTAA TACTTTTATA AATCAACAAG TAGGATTAGT ATGATGTACA AAGCGCCCTT 1260 GAGTTTGCTT CAGGAGACTT CCTCCTCTGT GTGACCACAA GTATATCACA TCGGCCACCT 1320 GGGCTTTTGT TTCCTTATCC ATAAATCCTT TCTTTAAGGG GACATCTTAT GGGTTCCTTT 1380
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