Tag | Content |
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EnhancerAtlas ID | HS116-35983 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chrX:100705160-100706630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MITF | MA0620.2 | chrX:100706066-100706084 | ATAGGTCATGTGACCCTC | + | 6.45 | MITF | MA0620.2 | chrX:100706066-100706084 | ATAGGTCATGTGACCCTC | - | 6.45 | TFAP2A | MA0003.3 | chrX:100705428-100705439 | TGCCTGAGGCT | - | 6.32 |
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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 |
GH0XI101449 | chrX | 100704701 | 100707540 |
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Enhancer Sequence | AGCCAGCACA GCACTGGGTC TTGCCCAAGG CCCTCTGTAA CCACTACCTG GCTACCACCT 60 ATGTTTGCTC AAAGCCCTAG GGCTCTACAA TCAATAGGTG GCAAAGCCAG TTAGGCTTGT 120 GTCTTTCTTC CCTCCCCTTC CCACAGGCAG ATAAGCCTCA CTCCATGGTC ACTGCCACCA 180 CAGGCCCATG GGGAAGTACT TCCAGATTAC CATCAATGTT CACTTAAGGC CCAAGAGCTG 240 TGCAGTCAGC TTGTAGTGAG TGCTTCCATG CCTGAGGCTC GTCCTTCAGG GCAGTGAACT 300 CCCCTCTGGC CCAGGGCAGG TCTAGAAATG CTGTCCATGA GGCAAGGCCT GGAATCAGGG 360 ACCCCAAGAA CCCACTTTGT GCTCTACTTC CAAGGACCAA GCTCATACCT AAGGTGCAAG 420 AGAAAGTTCT CTTTACTTTT CCCTCCGCTT TTCTCAAACA GAAGCAGTTT TTCACCATAG 480 CCACCAGAGT TGGCAATGTG CTGGGTCTCT CCTGAAACCA GCACATCTCA GAACCCAAGG 540 CCCATAGTGT ACTTTCTGGA TATTGCTGCT GGTTATTCAG GGATCCAGGG CTCTTCAGTC 600 AGCAGGTGAT GGGTCCTGCC AGGACAGAGT CTTTCCCTTT AAGGGAGTGG GGTCCCTTTT 660 GGCCCACAGT GTGTATAGAA ATGTCATTTG GGAGCTAAGG CCTGGAATAG GGGCCTCACA 720 ACTCTGCCCA GCACCCTATC CTACTGTGTC TGAGCTGGTA TCCAAGATGT AAGACAGTCT 780 TCTTTACTCT TCCCTCTCCT CTACAGAAAT GGAAGGAAGA GTCTCTTTTA AAGCTGTGAG 840 CTGTCTGCCT GGGGTTGGAG GTGGGGTGGC ATAAGCGTTC ACTTAGCCTC CCTGGCTTGT 900 GTCTCAATAG GTCATGTGAC CCTCAGTCTT CTGGCTCTGG GCCCAGTTCA GCACTAGGAC 960 ATGCCTAGGA ATTGCAGTCC TTTTGGCCTA GACTGTCTTT CAAGTTTATT TAGGGCCCCA 1020 GAACACTTTA GCCTGTGGTG ATAAGGCTTG TCAGAACTCA AGTTCTGACC ACTGGGATGG 1080 GTAATTTCCC TCTGGCTAGG GATGGTCTAA ATGCTCCCTC TGTGGGCAGG CATCAACTGA 1140 GTTCAGCCTG GTTTTGCTTT CTGCTATAAC GGGGCATCAC TGAGTTCAAT GCTAAGTCTC 1200 ATGATCACTG CATTCTCCTT CTCCCAAGCA CATGAATTTT TTCTCCATGT CATGTGGCTG 1260 CTGCCAGGAG ATGGGGGAAG GGTGCCATCA GCAATTCATG ATGGTCTTTC CTACCCTCTT 1320 CAGTGCCTCT TTCAGGGATA TGAAGTTAAA ACCAGGTACT GTGAGTACTC ACCTGATTTT 1380 TAGTTCTTTT GAAGGTGCTT TTTTGTGTAG TTGATAAATT TGGTGTTCCT GTTGGGGAGA 1440 TGATCAGTGG AGCCTTCTAT CCAGCCATCT 1470
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