Tag | Content |
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EnhancerAtlas ID | HS167-05866 |
Organism | Homo sapiens |
Tissue/cell | Retina |
Coordinate | chr6:41458710-41460180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HES2 | MA0616.2 | chr6:41458713-41458723 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr6:41458713-41458723 | GGCACGTGCC | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65317 | chr6:41459640-41460725 | Pancreatic_islets |
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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 |
GH06I041491 | chr6 | 41459641 | 41460725 |
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Enhancer Sequence | GCAGGCACGT GCCACCATGC CTGGCTAATT TTTGTATTTT TAGCAGAGAC AGGGTTTCAC 60 CATGTTGGTC AGGCTGGTCT CGAACTTCTG ACCTCATGAT CCACCCACCT CGGCCTCCCA 120 AAGTGCTGGG ATTACAGGTG TGAGCCACCA TGCCCGGCCA GGAAGTGCTT TTAATGATGA 180 GACTTCTATT CAAAGACCAG TGTGTGGGGA AGGCTACGCC ACAGTGGGGC TGGCAGACAG 240 CATGGACTGC GTCTCTACTG AGTGCCCAGC CCTGGAATCC CAAAGGGGAT AAACTCTGTC 300 CTCAAGGAGC AAACTAACAA AAAAGTGAAA AACAGCACAG GGGAATAGTG GGCGTCATGG 360 GGGTGGGGCG GGGGGGTAGG TGCAGTATGA GCATCTGGGG TAAGAGTGTC AGCAGAGGGA 420 ATAGTGAGTG CAAAGGCCCT GAGACAGGAG TGTGCTTAGC CTGCCAATTG TGTCCAGGGA 480 ACTGATGGCA AGAGAAAGAA AAATAGGAGG CATGTTAGAG AAGGTAGGCG CAGATCATGT 540 GGGACCCTGC GGCTGCTGTA AGAGCCTGGC TCTTCCTCCC AGTGCAATGG GGAAGCAGGG 600 GTAGGGGTGC AGTTTAAGTA GAAGACTGGC ACCGTCTGAA TTCTACAGTA TCTTCCTGCC 660 ACTCTGTGGA AAGAGTACCC CATGGGGGAA GGGGATGCAG GAAGACCAGG GAGGAGGGCC 720 CCACAGTCCT CCCAGGGAGA GGAGGTGAAG ACAGGAACCA GGGGCCCACC ATAGAGGGGG 780 TGAGAAGTGG TCAGATTCTG GACATATTTT GAAAGTAGAG CCAACGAGAT GGCTTAAGAG 840 TTGCATGTGG GGTATGGGAA AAAGAGAGCA GTCAGGTATG ACTCCGGTTT TTTTGGTCAG 900 GAATCGCCTT TCCTGAAGTG GGAAGACTAC AGAAGGAACA GGCTTGGGAA CAGACCAGGT 960 TCATCTGAAC ATCGAACCTG CTGAATTTGA GGGGGCCGTT ATCAATGCCT GATGAGTGAT 1020 ATTAGAGGAA CAATCCAGGA GACTGATCCT GTGTCTGTTT AAAATTATAA GGTTTTGCTC 1080 ATCATGAATT TTTTGTTGCA TTGTTTGATT TCTTAAAATA TTGCATTAAC ATATGATTTA 1140 TCTTGGTTAC TGAAGTTTTG TTCCTGCCTC CCTTTAAATT TTGCACCCGA GTTGCAGTCC 1200 TGCCTGCTGC AGACAACCAT GTGGAATGCG GGGGTTGGGC TGACCTCCCG ATTCCTGGCC 1260 ATTCTCTGTC CACCATGGGC CAGTGATCTT CTGATCAGGA TCTGTGACAG GGAGGTGAGC 1320 TGAAGAGTGG TTACAGCCAG GAGGTCCTGG ACAAGGAGAA GGGCCTGTGT GGATGTGTGG 1380 CTGGCTGACC TAGAAGCAGC CAGAAGGGTG TGAGCCCATC AGCCCGCTTC GCCCCACCCG 1440 GCCCCGTGAT GGATGGCATC TGTCTTCTGC 1470
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