Tag | Content |
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EnhancerAtlas ID | HS176-27291 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr3:124858770-124859860 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Ar | MA0007.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | + | 6.07 | Ar | MA0007.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | - | 6.7 | NR3C1 | MA0113.3 | chr3:124859385-124859402 | TGGAACACCATGTGCCT | - | 6.05 | RARA(var.2) | MA0730.1 | chr3:124859003-124859020 | AGGTCACTCCAAGGACA | + | 6.17 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27311 | chr3:124858008-124861858 | Esophagus | SE_32613 | chr3:124858836-124862530 | GM12878 | SE_46094 | chr3:124857933-124861421 | Osteoblasts |
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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 |
GH03I125139 | chr3 | 124857957 | 124863844 |
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Enhancer Sequence | TTCTGAAGCC TCTCTGGAGA GCATGGACCT TAAGGTTCGA GACCTCTACT CTAGCAGCTA 60 CATCTGCACG TGAGATTGTC CCGCCAGGAG GCACCTACAA CTTCCCAAGG CCTGACTGCC 120 ACCATGCCCT GCCTCAGAGT GGACAGCAGC CCTGAGAGTG ACATAGCCAA TAATGTCTTC 180 ATGCCACAGT CCTTGCCAAG CAATGGCCAA GACTGTGTGC ACAGAGATTG TGCAGGTCAC 240 TCCAAGGACA CCACAGGGCA ACCTCACTTC TGAAAATAAT GCTGAGCGAC CAGTGACTGA 300 ACCCTTCCTA CGTGCCAGCC ACTGAACAAC AAGACCTTAC AATGTCATAC TTGTACGATG 360 ACTAACTGAG GACACTGAGG CTCCGGAACG TGAAAAAGCT TGTCCGAGGG TTACATAGCC 420 AGATCTGCCT GTATTTCACC CACTGCCTCT CCCGGTGGCA GAAGCCAGGC CTCTCTCCAG 480 GAGGTGGGTT CCCAGGCCCT GGCACTGCAC CCCCTTACAG CACAGGTTGC CTTTCAGCCC 540 CAGGAAACAT GCCCACAGAG ATCATGGCAT CTCCCCCGGC CCCATTTGTG TAGGGCAGAC 600 AGGAGTCCTA TCCTGTGGAA CACCATGTGC CTACCGGTAT GCAACTGGCT GGAGCTTACA 660 CAGCTGGGAG GACACAGCCT GTCCTGGACC CCACATCTGA GTGAATTCAG GCCTCCATCT 720 ACCACACTGA CCCTCTGTAA TCCATCCCAA AGTCATTCCC CAGGAATTTC CTTTTTTTTT 780 TTCTTTTCTT TCTTTCCTTT TTTTTCTTAA AGAGGCAGGG TCTCGCTCTA TCACCGAGGC 840 TGGAGTGCAG TGGCACTATC GTAGCTCACT GCAACCTCAA ACTCCCAGCC TCGAGCAACC 900 CTCCCACCTT GGCCTCCCAA AGCACTGGGA TTACAGGCGT GAGCCACCAC GTCTAGCCTC 960 CCCAGGGATT TCCAACACTT GTTTTTTGAC CTCAGAAGAG TCTCTTTGCC TCTCTGTTGG 1020 GCTTTCAATT CCTCTGCTGG TGAAACTGAG TCTTGTGGTC TGGGGTCCTG TCATCTGACA 1080 TCTTTCAACT 1090
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