Tag | Content |
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EnhancerAtlas ID | HS176-28628 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr4:17490920-17492280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX6 | MA0069.1 | chr4:17491096-17491110 | AAATCAAGCATGAA | - | 6.2 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_05190 | chr4:17489853-17497659 | Brain_Cingulate_Gyrus | SE_06499 | chr4:17490010-17497652 | Brain_Hippocampus_Middle | SE_07155 | chr4:17490593-17493004 | Brain_Hippocampus_Middle_150 |
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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 |
GH04I017490 | chr4 | 17491645 | 17492530 |
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Enhancer Sequence | CCTCTGTGGG TCTGTGGCTC AGCACGAGTT CAGACACAAG ATCCCAGATG TTCCATCTAG 60 AGTAGGTCTT AGATCAGTAT CTCAAGTGTG GTGGGAGTGT CGGCCTTTAA AAAGAAATTC 120 AAACACAAAC ACAATTCAAA GCTTGATTTC CTCTACAACT TCAATTTTTT TCCTGCAAAT 180 CAAGCATGAA GCATGATTCC TGGCATAGAC AGAAATAACT GTCAGCACAC CAGTTAAGAC 240 CATAGGTTCT GCAGCCACAC CACTTGTGTC AGATCCCGGC TGTGCTGTGT GACCTTAGGC 300 GAGTGACTTA GCCCCTGCCA TCCCTCCAAG TCTCTAAGCC TTAAATAAAA ATGACAGCTC 360 CTCCCTCAGA GTTTGCTATG AGCATTAAAT AAGAGTTATG AAGTGCTTAG AATGGTGACT 420 GGGACATAAA AAGTGTTCTG TAAGTACACA TTTCAAACAT AAAACGCAAG TCCCAAATTT 480 CTCCCGATTT AATTTAAATG AGATTGTGAC ATCAGGCCAG AAGCACACTG CTAACTTCAC 540 AAACATCTCT TATAAACAGT CGTCAAAGCA GTTTACACAG AGGCACTACT GGGTCAGGCT 600 GTCACCTTGA CCCTCTCGGC ACCCCTGCTC CCTGTGGGCA GGGATCCCAT CTTTGTCCTC 660 ACCGTGACCC CAGAGCCGAG GGCAGCACCT GGCCCATAGT GGGTGCTCGA TGAACACATG 720 CTTACTAACT AGAGGGGCTT GAGGAACTGA TACCTAAACA AACACAAAAG AGGAATTCAG 780 CTCTCTGTCC CATGAGCGTT CAAATGCCAC CCATATTCAC AAATGGGCAA AAAGGATTTC 840 GGAAATTAAA GGGCACTTTC TGTGGGTCTG TGGCTTGACA CAGATTCAGA TATGTGCCCC 900 CAGGCCATCT ACGTGGTGTC CCCCTCCCCC ATGGAGTCTC CTCATCACAG CAGTAAGGAC 960 ACAAACTGCA GCTGGGGATC ACTGAGCACT TGTTATGGCC AGACACTGTG TTGAGTGCTT 1020 GCCGCACACT ATCACGTTTA ATCCTAACAA GCATGATGGA CCTCATGATA CAGGTGGGGA 1080 AACTGAGGCC TCAGCAGGTC AATAATGTGC TCAGCATGGC CGGTGGTGAG GGAGCGAGCC 1140 AGGATTCATG TCGGCACTAC CCATTCTGCC ACTGTGCTGC CTGTCTCCAA GTCCAGCTAC 1200 TCTGAGATTC CGTCTGATGT GCAATGCATC CTCAGAGTCC CAGAGACCTC CCAAGACCAC 1260 CCGGATTGAC GATCTCAGGG AACACAGACT TGTCCTCTGG ACCACAGCAG GCAGAGAATA 1320 GGGGCTGGAA GCTGCTCAGT CATGGACATG TCTGTAATAC 1360
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