Tag | Content |
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EnhancerAtlas ID | HS095-23846 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr5:43429220-43430470 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP2 | MA0593.1 | chr5:43429401-43429412 | TTTGTTTACAT | - | 6.14 | Foxd3 | MA0041.1 | chr5:43429462-43429474 | GTTTGTTTGTTT | + | 6.32 | MEF2A | MA0052.3 | chr5:43429780-43429792 | TTTATTTTTAGA | - | 6.07 | PRDM1 | MA0508.2 | chr5:43430240-43430250 | TCACTTTCAC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_33973 | chr5:43425153-43430699 | HCC1954 |
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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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Enhancer Sequence | GATATTTAAG TGGTGGAGGA AGAGCTTCTC GGAGAACAGC ATGTGCATAG GGAGCCAGAC 60 CATGTTCAGT TCTAGGCACT GCAAACAGTC CAGCGCTCTG CGCAGAAGCT GGACTTGATC 120 CAAAAAGGCT ACAATCCAGG GGGCAGGGAA TGTGTCTGGT TTGCTTAAGG TAGGGGTGAC 180 TTTTGTTTAC ATATTATTTT TAGTGGGTTT TTTGTTGTTG TTGTTGCTGT TTTGGTTTTT 240 TTGTTTGTTT GTTTTTTTGA GACAATCTCT CTCTGTCGCC CAGGCTGGAG TGCAGTGGCC 300 CAGTCTCGGC TCACTGCAAC CTCTGCCTCC CAGGTTCAAG TGATTTTCCT TCCTCAGCCT 360 CCCTAGTAGC TGGGACTACA GGGGCCCACC ACCTGTATTT TTGTAGTTTT ATGCCCCGCT 420 AATTTTTGTA TTCTTAGTAG AGATGGGGTT TTACCACATT GGCCAGGCTG GTCTTGAACT 480 GACCTCAAGT GATCAGCCCG CCTTGGCCTT CCAAAGTGCT GGGATTACAG GCATGAACCA 540 GTGCACCCAG CCTTCAGTGC TTTATTTTTA GATTGTAAAT AGCCCATATT AAGAGGCAGC 600 TCACATTATA CTGAGTCTGT ATAGAGGCTT CTTAGCTGCT ATGCCTCTAG CCTCTGAAGT 660 TCTTGATGGG AAGTGTACAT AGCTAAAAGA CACCAATTAA AATCTGGGAG CTTTTGGATT 720 CAGCTCCCAA TTATCACCTC TAGAAAGAAA GGCAAGCCTG ATCATGCCAT TCTCAGGCTT 780 AAACCTTGCA ATGCTTCTGC ATTGCCTCAA GGTAAGTTCC TAAGTCCTTA AAAGGTATAC 840 AGGGTTCTCC AGGACCCAGT TCTGGTTAGC TTACCGACTT CAACTGTTGT CACTCTCCCA 900 CCTCAAACAC TCTGCTCCTG CGTTTCCTAC AACCCCACTG ACCAGCTGCC ACTCAAGGCT 960 TTTGTAAATG CTATTCCCTC TGCCTTCAGG GAGCTTCTCA GCAGTTCTCC ATCACCTTAT 1020 TCACTTTCAC CTGAAGACCT CTTGCTCAGC TATTGGTTCT CAGGGAGCTT CCCTGTCTGC 1080 CCTAGGGGGA CCTCCAAGCC CCTGTGCTTG ACCTGACTGC AGCACTTACC ACCCTATACT 1140 GAAATGTCCT GTCTCCCTGT CCATCTTCCA ACTAGCCTAG GAGATATTTT AAGATGGGGC 1200 CTGGTTTTTT CCACCATTAG AATATTAGTT TTTAATACAA GGCCTGCTAC 1250
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