Tag | Content |
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EnhancerAtlas ID | HS116-08730 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:104571100-104572480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:104572299-104572320 | AAATTGAAAATGAAAAAAAAA | - | 6.53 | REST | MA0138.2 | chr12:104572252-104572273 | TCCAGCACCAAGGAGACTTAC | + | 6 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 104571112 | 104572475 | chr12 | 104571400 | 104572400 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I104177 | chr12 | 104570921 | 104572788 |
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Enhancer Sequence | CTCCCCAGGT GAAAAGTGAT GTGAAGTCCC CCTCAGAACC CAACCTTACC TTGACCACTC 60 ATTTTAGGAA GTTCCCTGCC CCCTATCCCA TCACTTCTTT TCATTGCACC CAGAATCAAT 120 TGCCTTCATA CACTTAATAC AGTTCATTCA TTTTACTTAG ATATACATTT GTTTGTTGTC 180 TGTCTCCTAT ACAGTATATA GAAAGCTGCA TGGTGAAATG AATGGTGTCT GTTCCACTTC 240 ACAGTTTATA CCCAGCATCT AACTCAGGAC TTGGCACATC ACAGGAGCCT AATAAATATC 300 TGTTGAAAAG TGAACGAAAT AAAAGCTACA CTTACGCAAC AAGACCTCCT GACATTGTTT 360 TCCAGCAGCC AGCATCTTCT GTTCTGAGAA TGTGGTGAAC TTTCCTGTAT CTTAATGGAT 420 GATTCATTCT GTGGCCAATT GGCCGGGGGA GGGCAGTAGC TCCTTGTTTC AAGCTCCTGC 480 CTCCCTGTGC CTCTTCTGTT TATCATTTCT GCCCTGATCT GTTGGCAGTG GCCAAACCCC 540 ATGGACTCTC CCTGGGTTTT GCCTCCAGAA TCCCACCCTC CTGTTACAGC CCTGGTGGCC 600 TTCGAAGTTT CTTGCCAGGA TTCCCACCCT GACCTCCTCA CTGGGCTGCT TGCCAGCAGT 660 CTTGCCCAAT TCCACCCCCA TGTTCCCCTC AACTGCCAGA GATAGTATCG TTAAGATATT 720 TGAAAAATTG ACTCTAGAGT CTAAAGACTC CCCTGCTCTT CAAAACCCAG AGATAAGATC 780 AAGTCCAAAC ATTTTGGCGT GAGGTTCAAG GCATTTCACA ATCTGCCGGG AGGTCCCTCT 840 CCCAGCTCCT CTCTAATTAC CCAGCCCACT TCCTCCCAGC CTGGGTTCCA GCCACAGAGA 900 ACCTTCTGGC ATTCAGTGAA TGCGTCTGAC AGCCAGAATG CCAGCATTTG GTGCCAGCTA 960 TGCCTTTTGC CTGGCCTGGC TTTGCCTCCC CTCCTTCACC TTGAAATTCT CCTTCTCATC 1020 ATCCATCTGA CCTGACTTGA AATTATGCTC TCAGGAAGGG AGGCCTGCCC AGCCTGGGTT 1080 ATTCGTATCT CTACTAAAGC TCTCATCACT TCATGCCATA AGTCCGCAGT CTCAGCCTCT 1140 GCTGCTATGG TTTCCAGCAC CAAGGAGACT TACTAGAAGA GATGAAGGAA GAAAAGAAGA 1200 AATTGAAAAT GAAAAAAAAA AATGAAGTCT ATGCCACCCT ACCCCAACTT CTTATTTTCT 1260 TCTGCTTCTC TCTTCCATTG ACTAGTTACT TTGAAAGGCC TTTTATGGGG AACATCTGTT 1320 GTGCTTGTCT GCCTGACAGT CCTTCCCTTT TCTGGAAACA GCACTCTTCT TTCCTATGGG 1380
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