Tag | Content |
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EnhancerAtlas ID | HS095-07150 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:53312000-53312860 |
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) |
DMRT3 | MA0610.1 | chr12:53312644-53312655 | TTTGATACATT | - | 6.02 | MEF2C | MA0497.1 | chr12:53312485-53312500 | GTGCCTAAAATAGCA | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47304 | chr12:53312191-53313337 | Panc1 |
|
| 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 |
GH12I052918 | chr12 | 53312254 | 53312405 |
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Enhancer Sequence | GAAGAAGAAG AAGAAGAAGA AGAAGAAGAA GAAGAAGAAG AAACAAAACA GAGTCTGCGT 60 CAACTGGGAA GTTCATGAGG AGGGTTCAGG CAGAAGGTCA AGGGGCCTCT ACTGTATCAG 120 CTGGGTTGTT GGAGCCTCAG AAACATGCAG GCCTACTGTA TGCGCTGCAT GCATCACCTC 180 ATTTAAATTC ATAAAGATCC CACCAGGCCG AGATGGAAAA GTGCCTACAT TCACACAGCT 240 GTGAAGGGAA GAACTGGCAT CTGAGCCCCG CCAGACAGAC GCCGCGCAGG TGCAGCTGCC 300 CCGAGCCTGC CCATGCATGT TCTGCTGCCC CAAAGCCATG TGTGACCAAA ACCCAAAGGA 360 CAGAGGGTGC AACCAGAAGA ATTTCGCAGC CACTTCCTAA TGGTGTTAAG AGTTACTTCA 420 CCAGCTGAAA ATGCAGATAG TAACAACTAC CTCAGAAGAC TGACATGATC ATCAGGTAAG 480 GAACAGTGCC TAAAATAGCA GGTTTTCAAG ACATGTTAGC TTGACTCTCA CCAACCCTCC 540 CTGCTTGTCC CCCAGCCTTT CCCAAAGCCT TTCTCCACAC AATTTCCCCC ATTCCCTCAC 600 CACCTTCAGA CCACCCTCCC CCATGGAACT TGTGTTCACA TCACTTTGAT ACATTTGCCT 660 TGTGAGAGTT TAAGCCTTGT GTTTCCCTGC ATGAAATAAC CTCCTTGCAG AACAGAACAG 720 TGTCTGCTGC CTCTTCCCAG GGTAGGTGGT CAAGTGGAAG AAAGTGCTAG CTCAGCAGGG 780 TGGAGGGTAA CTAGGAGGTG GCAATTGGGT CTATAAGGAG GAGCTTATAG GATAGTAATA 840 AAGAAATAGC ATGTAAAAAT 860
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