| Tag | Content |
|---|
EnhancerAtlas ID | HS116-29270 | Organism | Homo sapiens | Tissue/cell | Left_ventricle | Coordinate | chr6:31197500-31198560 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr6:31197809-31197830 | TCTCTCTTTCTTTTTTTTTTT | + | 6.07 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 31198131 | 31198245 | | chr6 | 31197627 | 31197769 |
| Enhancer Sequence | AGGATGGAGA ACTCTCATTC TCAGCCCATG ACCTCCATGG ACTTGGAGAA AGACTCAGCC 60
TGGAGATGTG TGAGGCCTCC GACCTGGAGC AGCACCCGCC CCTAAAGACC AGGCACAAAT 120
CCCAGCACAC GGGGGGATCC AGACAAATAC ACAAGAAATG ACCACAGCAG GAACTTTATT 180
GAGCACGGAG CAAGGGTGCA CACCACTCAG CACCTGCCCC TCCACCTGTC CTTCTCTCCC 240
CACCTGCCTC TGCCCCAGCA CAGCAGGTCC TCAGAATCCA AAAAGAGAAC CTAACCTGCA 300
TGTTCTCTCT CTCTCTTTCT TTTTTTTTTT TTTTTTTTTT GAGACAGAGT TTATCTCTTG 360
TTGCCAGGCT GGAGTGCAAT GGCGTGATTT CGGCTCACTG CAACCTCCAC CTCCTGGTTC 420
AAGCAATTCT CTTGCCTCAG CATCCCGAGT AGCTGGGATT ACAGGCAGCT GCCACCACAC 480
CCAGCTAATT TGTGTATTTT TAGAGATGGG GTTTTCACCA TGTTAGCCAG GCTGGTCTCG 540
AATTCCTGAC CTCAGGTGAT CTGCCTGTCT TGGCTTCCCA AAGTGCTGGG ATTACAGGCG 600
TGAGCCACCA CGCCTAGCCT CCATGTTCTC TTAATAGTTT GTAATATCTT ATCACAGCTT 660
CAAAGAAAGG ATATGAGAAT AATAACTCAT AGAGCAAGAT ATCTGTTTAG AGTGAGTGAG 720
TCACAGGGGA GATCTGGGAG GGAAACACTG CAACTCTTTC ATTCCCAGAA AAAGAAGGTT 780
GATCCAGGGA AGGGGACACC GGGCCTGGAT ATTGGGATTA TGTGGAAGGG GTTCTGGGAC 840
ATCAGGGGAA TGGGCCCCTC TCCCTGTATC CTTCCTGGGC TATGCTTGGG AGGAGACACA 900
GTTTATCAGC TGTGCAGCTG GGGGAAGAGA AGTCAGGGTC CAGAGACAAG GGGAGCTGAG 960
AACAATCTGT GTCTTGCTGG TCTGCAGAAG GCAGCTCTCA AACTGTAGAG AACAGTTTGG 1020
GATGATGAAA ATGTTCTAAA ATTAGATATG GTGATTTAAA 1060
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