Tag | Content |
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EnhancerAtlas ID | HS150-07958 |
Organism | Homo sapiens |
Tissue/cell | NT2-D1 |
Coordinate | chr3:171926490-171927660 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr3:171927353-171927368 | CTGATTGGTCCATGG | - | 6.98 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_09145 | chr3:171926298-171933667 | CD14 | SE_37908 | chr3:171926030-171931693 | HSMMtube | SE_45552 | chr3:171925626-171933380 | Osteoblasts | SE_47161 | chr3:171926466-171929583 | Panc1 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH03I172208 | chr3 | 171926381 | 171929412 |
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Enhancer Sequence | TTCTGGGCTT CTTCTGCCCA CTTGGCCTGG ATCAGGCAGC ACCACCGGCC AGGATCCTCC 60 CCTGCCAAGG GTGCGCCAGT CACGGAGCGG CGAGGGGTGT CTAAATGATT GAGCACAGGG 120 TCCGGCCACT GTGCACAGCT AGGCATTCTG GCTGTTGCAG TGGGGTGGGC AGCTCCATGC 180 ACCAGCATAG GTGCTGGCTC CGTGCAAGGC TGTGGCTGGA CCAGACATAC CACAAGCTGT 240 GGGTACCAGT GTCTGGATGA GGGGAACACA GTGGCGCCTG AAAGCTTGGA GATGCCAGGA 300 ACCACAGAGC CCCAAAGAGG GTGTTACAGC GTGTCACAGC CCTGGCTCCG GGAGCCCTGA 360 GTTCTGGGCT CTCAGTAGGG CCACACCTCT TCTCTCCTCA TTGCCTACAG TGCGCAGTGA 420 GCGGGGGTGG GGGTGGGGGT CGTGTTTCAG CCTGTTTGTG TTACAGCTCT TTCAGTCATG 480 CTTGCCTCTG GCTCCTGGGC TGGTCCAGCA CCACCACTGC TTCCTGTTGC ATGAGGTGGC 540 TGCCTAGTGC TGGCAGAGGG CGGGAGGGCT GTAGTGTTAC AGCCCCTTTA GCTGCCGCCC 600 ACAGCTGGGC AAGCTGGCCA GGAAAGTGTT ACAGCTCCTT TCGTTCCTGC TGTTTGGTGG 660 GTCTCGAGTT TTTCTTCCAC ATCCAGGAAG AATGAAGTTA CACGGGCAAC TGGAGGGTGA 720 GCAAGGCCGA GAGGAGCTTT ATTGAGCAAC AGGAACAGCT CTCAGTGGAG AGGAGACCCA 780 AAGTGGTTAG CACCTATCCA CAGACAGGTG ATGAGTCGCT GAGTCTGGGG GTTTTTATGG 840 GCTCAGAAGG GAGGGCATGT GTGCTGATTG GTCCATGGGC GGCCACAGGC GGGCCTGGAA 900 AAAGCACCAT CCGATTATCC GAAAGGCATC AAGGAAGTTC TCACTCCCAG TAGCCGACTC 960 CACCCAGAAC TGGCAGCCTC GACCATAGGC TTCAGGCCCT CCCTGGCTTA AAGGTGGAGT 1020 TTCACCAGGG ACCTGCCCCT TCCTGCCTAG GAAACTGTCT GCCTCCCACC ACTATCAATA 1080 TGCCATCCAT GGCGCCCAGG CTGTCCGGCC CGAGGGGCAC CTGCAGGCCC GCACTGAACT 1140 GCCCTCAGCC CCTTGGCCTC CTTCCCATGC 1170
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