Tag | Content |
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EnhancerAtlas ID | HS116-19320 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr2:134338230-134339650 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr2:134339087-134339098 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr2:134339087-134339098 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr2:134338553-134338574 | CCTTCCTCTTTCCCTTCCTCT | - | 6.75 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH02I133580 | chr2 | 134338179 | 134339513 |
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Enhancer Sequence | TTAAGCATTT TCCCCACAAG CTTTAATCAC CTCTGAGTAC CCTAGAAGAC GCAGTGCACA 60 GGTCCTCAGA GAGAACATTT GTGCATTTGT GGACAGACTT TGGTTTTGCA TGTGAAGCTT 120 CCATCCCAAA TACAAAATCA CACCATCAAA GACATTCATT ATTTTGTAAG ATTATGTCTT 180 ATGAATATAT ATTCAGTACA AAGTTTCTCT CTCTCTCTTT GGAGGAGAGT TTCGGAAATG 240 AATAGCTCCA AACTCAACAG CTACTTGCAA TCAGTTCTGG AAACCCTAAG TGACAGCTTG 300 TTTCTTCCCT TTTCTTCCAA CCTCCTTCCT CTTTCCCTTC CTCTTGCTCA TCTTTTTAAT 360 ATGACTTAAG TAAGGAAGAA CTTAATGATA TCTACCTTAG TCCCTAACAG TTTTTTCAGA 420 ACTCTGTGTC TGAAAGAATG ATCTCATCAC AAATTAATCC TCCATTGCTC CTAAAATAAA 480 TCTGTATAGA ATGACGACAT CTGTTTCCAA CTCTACAATA TGAGTTTAAA AAAAATCTTA 540 AAAGTAAACT TGGGAAGGAA ATGTCTCAGA TGCATTTGAG TTCCTGGTGA ACAGCATCAA 600 AAGGCTTTAT GCTGGTAAGA CAGGGCCAGA GATGGTTATC TTATTGGACA CCTGTGCCTC 660 ATCCCCATCC ACTTCCTGTT GTAAGGGATT CTTCCTATGG AGAGTGAAGA ACATGCTGGC 720 TAATTTAAGT CCCACTGTTC TTCTTGGTGG AATCTCAATG GCTGTCCTGA GCCCCAGGTG 780 TCAGTTTGGG AATGCATTTT CACAGGGCAG GCATCTGGCC CTGAGTCCTT GGCAAACCAA 840 CTGTGACAGG TTCCTCTGAC AGCTGCAGTG GCAGGGCTGG GCCTCCAGGT GATTAAATAA 900 TCCTGCTTTC TGGCCCAATC ATGTGTTTGG ATTGGACCCA TTTCCCTGGA ATGGGGCTGA 960 ACCAAACACA GCTGCTGCTC ACTGACCACA GTGAGGTGTC TATGGGCTGA GCACTCCCCA 1020 CCCTAAAATT GTGAAATGTC CCTTTTTCTT TCTCAGACAA CTCAAACCTT CAGTTATCAC 1080 AGACATGCCC CTGGAAATAT AAGAACCTCC ATCTGTCTGA AATGGAGCTG AAAGTTCACT 1140 TTTCGTTGTA AGTATTGTTA AATTTGATAG CTCTGCTTTG AAAAGCAGGG GCCATTTCTA 1200 ACGTTAGCTA GAAATATTCC TTTCTTTCAA TAGTAGTAGG CATGCCCATG CAATACACAT 1260 TTGACTACAT GTGTACACCA GATGAAGAAA TGGATCAAGA GGATGTATAC TCAATGTATT 1320 TACATTTTCC AAAGATATGA CACCACGTCC TGGAGAAAAA AATTAAAATA CCTCTTTGTG 1380 GTGAAGCTTA GTGTTGCAGA CACACAAATA TCAATGGCCT 1420
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