Tag | Content |
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EnhancerAtlas ID | HS105-42426 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:28940050-28940990 |
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) |
NFAT5 | MA0606.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr2:28940106-28940116 | ATTTTCCATT | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_02169 | chr2:28939958-28940678 | Aorta | SE_41111 | chr2:28938705-28940799 | Left_Ventricle |
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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 |
GH02I028713 | chr2 | 28936139 | 28941575 |
|
Enhancer Sequence | TTGATGTCCT TTACTTCAAG TTAAGCCTGG TGTTTGCTTT AATCACAGCA GAAAGCATTT 60 TCCATTTCAG GGAAAGGAGA GAACAGGCCA TAAACCCTGT CCCCTGTTTG TTCTCCAACT 120 ACCCATTTTT GTCCTTTGCC CTGCCATGTC TTTTCCCCCT CGTTTGCTTC TCCTTTCTTT 180 GTTGATTTCT CAGTTCTTTT CTGGCCTCAC TCAAAATGGC AGAAATTACG CAACCTAGTA 240 CTTTTTTACA CAAGCTCCTT TAGTGTCAAG GATTCATCAA GTGCCTGCCA TGTGCCGGAA 300 CTGTTCTAGA TGCCGAGAAT ACTACCATGA ATGAAATAGA CAGAAATCCC GGCTGTCATT 360 GGGCTTTGTC TGAGGGCCAT TGGGGAAGGC CTCTCAAAGG AAGTGATAGC TGAGCTGGGA 420 TCTGAGTCAT GAAGAGGAGT GAGCCCAGGG GACAACAGCT GCAAGAGTGT GCCAATGGGA 480 GAGACCAGCC CAGCAAAAAG GAGAAGCATA AGTCTGGTGC ATTCCAGGGA CAGGAAGGAA 540 TGGGGCAGGG TGCCTTTAAG AGAAAAGCAT CAGTTTGGAT GAGGAGGGAT GTAGGGTCGG 600 GAATACAAAA TAAGAGTAAT TATGGCTGGG CACAATAGCT CACACCTGTA ATCCCAGGAC 660 TTTGGGAGGC CAAGGTGGGC GGATCACTTG AGGTCGGGAG TTAGAGACCA GCCTGGCCAA 720 CATGGCGAAA CCCTGTCTCT ACCAAAAATA CAAAAATTAG CTAGGCCTGG TGGTACGTGC 780 CTGTAATCCC AGCTACTCGG GAGACTGAGG CAGGAGGCAG AGGTTGCAGT AAACCAAGAT 840 CGCGCCACTG CACTCCAGCC TGGGCAAAAG AGTGAAAGTG TGTCTCAAAA AAAAGAGAGA 900 GAGAGAGAGA GAGAGAAATT AACTTAGGGT GAAAGGCATT 940
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