Tag | Content |
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EnhancerAtlas ID | HS116-21825 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr21:47547470-47548810 |
Target genes | |
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) |
BHLHE41 | MA0636.1 | chr21:47547742-47547752 | GTCACGTGAC | + | 6.02 | BHLHE41 | MA0636.1 | chr21:47547742-47547752 | GTCACGTGAC | - | 6.02 | MITF | MA0620.2 | chr21:47547738-47547756 | GGATGTCACGTGACCTTT | + | 7.42 | MITF | MA0620.2 | chr21:47547738-47547756 | GGATGTCACGTGACCTTT | - | 7.42 | USF1 | MA0093.2 | chr21:47547742-47547753 | GTCACGTGACC | + | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_54792 | chr21:47547628-47549365 | Stomach_Smooth_Muscle |
|
| Number: 1 | ID | Chromosome | Start | End |
GH21I046127 | chr21 | 47547655 | 47549150 |
|
Enhancer Sequence | GGCGTCCTCC CCCAGGGTCC ACATCAGCAG CAGGGGCACC TGGACCCTGA GGGCAGGAAC 60 CAGACCTTGG CTCCTCCACC CACCCCCTCG TTCCTGATGG GGCAGGGAAG TCTCGGGACC 120 CCATGATGGG CGACATGGCG ATGGTCACTG TGGGTGCTTT GCTATCAGGT GGGGGGCCTT 180 CCTCTCCACT CTGGGTCCAG TGTGAGTGGC CGCTATGGCT TCCCCTCCAC TCCAGGTTCT 240 ATCGTGAGTG GGTGGGTGCT GCGTCTGTGG ATGTCACGTG ACCTTTCCTC TTTAGCCTAT 300 CATTGTAGTT GGGAGTTAGT TAGCCCGTTG AGCGTCATTG AATTTCCAGT GTTGAGCCAG 360 CCCTGCGTGC CCGGGATAAA CCCACCTGGC CGTGGTGTGT GGCCCTGTTT ATGCACGTGG 420 GCCCTGATTC GCTGATGCCT GCCTGAGGGT TTGCGCTTAT CGGCGACATC AGCCTGCACT 480 TTTCTTTTCT CGTGATCTCT CTGGTTCTGG CCTCAGGGTG ACGTGGGCCT CGTAGGGTCC 540 TGTGGTGGCT CCTCCCCAGA CGGTGACATG GAGTGAGCCC ATTCTCCCTC CTGGGAGTGG 600 GTCACTCAGG CCACCAGAGC ACCACAGGGA AAGCAGCCAG GGAGGACACG GAGGCCCTTG 660 AAGCTCTGGC CTCTTCTGAG GCCTCCAGGA CCTGACAGTG AGTGGGAGCA GCCCTGGCAG 720 AACCCCTCCC CTCCTCTCGG CCGCCCTGAC ACCTCATCCC CGACACTCAG AGCTCATCCT 780 CCTTCCCAGC TGTTTCCAAT TTCAAAGTGA ACTCGACCTT GTGGCTCCAG GAGATGCAGC 840 AGGGACAGTG TTAAATCGGC TTTCACCAGC CCACACGGCC AGGCATCCTC CTCGGCCCTC 900 CTGGGCACTG GGTGGACACC ACTGGCTGTG GCCTGGCCCT GGCCTTCTCC AGACAGCCCT 960 GTCCACCCCA AAGCCCAGCC ACCCTGGGCC TGCAGCAGGC CTGTGGAGTT CTCAGTTGCG 1020 TGGGGACCAG AGGGTGCTGG AGAAACAAAC CAGACGCAGC TGAAGGCAGT CAGGGCAGGG 1080 CGCAATCAGC GATAAGAGCT GCATAGGGGC CACAGCGTAA CCTGAGCTCC AGTCGGTGGA 1140 AAGAAAAGGC AGAGACGTTG CAGAGGCCAG GTCTGCTCAG GGGAAGACAG TTCTGGGTGT 1200 AGAGGACTCA CATCCCAGAG AGGCTGAGGA AGGGTTTACC ACCGCAAGCT TTCTCAGGCG 1260 GGCTCTTGAG GGGTGGCTGG GGTCTTCCTG GCGACGGGCC TGCGGCACTG GAAGCCCTAC 1320 TGGAGTTTGG CCTGTCTCCG 1340
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