| Tag | Content |
|---|
EnhancerAtlas ID | HS116-07867 |
Organism | Homo sapiens |
Tissue/cell | Left_ventricle |
Coordinate | chr12:11918170-11919990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr12:11918421-11918431 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr12:11918421-11918431 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr12:11918421-11918431 | AATGGAAAAT | - | 6.02 | | SOX10 | MA0442.2 | chr12:11919905-11919916 | TGCTTTGTTTT | - | 6.02 | | ZNF263 | MA0528.1 | chr12:11919445-11919466 | TCTTCATGCTTCCCTTCCTCC | - | 6.27 | | ZNF263 | MA0528.1 | chr12:11918994-11919015 | GAAGCAGGAGGAAGGTGTGGG | + | 6 |
|
| | Number of super-enhancer constituents: 23 | ID | Coordinate | Tissue/cell |
| SE_01754 | chr12:11918069-11920156 | Aorta | | SE_09138 | chr12:11895682-11929433 | CD14 | | SE_12874 | chr12:11918556-11920257 | CD34_Primary_RO01480 | | SE_13315 | chr12:11914238-11920650 | CD34_Primary_RO01536 | | SE_14048 | chr12:11917909-11920987 | CD34_Primary_RO01549 | | SE_25354 | chr12:11914277-11930036 | DND41 | | SE_25772 | chr12:11913943-11922646 | Duodenum_Smooth_Muscle | | SE_30380 | chr12:11917824-11920904 | Fetal_Muscle | | SE_30906 | chr12:11914521-11920257 | Fetal_Thymus | | SE_32458 | chr12:11910093-11922451 | GM12878 | | SE_39367 | chr12:11914420-11925956 | Jurkat | | SE_43859 | chr12:11917454-11920221 | MM1S | | SE_46110 | chr12:11915046-11920204 | Osteoblasts | | SE_49833 | chr12:11914096-11919206 | RPMI-8402 | | SE_51622 | chr12:11918249-11920506 | Skeletal_Muscle | | SE_54656 | chr12:11914202-11920959 | Stomach_Smooth_Muscle | | SE_58379 | chr12:11878906-11990784 | Ly1 | | SE_58837 | chr12:11874923-11935776 | Ly3 | | SE_59849 | chr12:11874575-11943335 | Ly4 | | SE_61023 | chr12:11869475-11929777 | HBL1 | | SE_61926 | chr12:11879670-11927640 | Toledo | | SE_62748 | chr12:11877030-11934459 | Tonsil | | SE_66238 | chr12:11914420-11925956 | Jurkat |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 11918792 | 11919487 | | chr12 | 11919566 | 11919967 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I011761 | chr12 | 11914429 | 11925846 |
|
Enhancer Sequence | TACTGTCCCT TTCAGAGCCC TGGCACATAC ATAGTGTAAT AAGATCAGAC CCCATCCCCC 60
TACCATTCCA ATGCAATCTA ATTGCAAAGT GAAAATCCAG GGCCGTCTTA GATCCTCATC 120
TGTCTACGTC TCTCTTGGTC CCCACTGCTT GATACGCAGT CTCAGGTTCA ATACCATTCT 180
CTCTTTTTGT GCTTTAGGTC TCTGTATTGT TTCCTTTTCA CCACTTTTTT TTTTTTAATG 240
AAGTGATTTT AAATGGAAAA TTAAAAACTT AACTGTGAAT CTGGCAGTTT CCTGCTAATG 300
CCTCTTTGCT AAGAAGCTTC ATAAAATACT GTATCTTATT CACTTCAGCA CAGCTGCTGT 360
GGGCTCTCAC CACTTAACCA TTCACAATAT GTCTGAGAGA TTAATTTTTG TAAGGCTGTG 420
GTTTGAGATA TCTCCCCCTT CCTTGTTTTA CTTAAAATCC TCAGTGGGAA AGCGTGCATG 480
GGGAAAAAAA AAACCACCAC CACCCTGGAT AAAAGGTACT TTGGTAACAT ACGTGCTTTA 540
GGAACTATAA TTTGTCATTT TATTTTCTTG TGCCCTCTTC ATTTGAAATG CTGCAGCCTT 600
TCTGCCAGAA GTCTCAAGTT TGTGTATGAG ACTGAGGGGG AAACGAGAGT AGGTACCTTG 660
TGCTGAGACT GTCCTGGGAC AGTCCCGTGG TGGGTGTGAG CGTCTGTGTG ATGCAGGTAT 720
GCTTATTTCT TCATGAAAGC CGCAGGTACT GGTTGCCTCT CGCAGGGTTA AAACTCTTGG 780
CGGCTCACAG GAGGTGATGA AGAGCAAGGG CACGGGAGAA TGAAGAAGCA GGAGGAAGGT 840
GTGGGCCAGG GTCGGTTTCG GTGGGGTCCC CACTTGCTGG GTGAAAGCTG AACTGTTTAT 900
CCACACATCC CAGCAGCAGC AGAAAGCCAA GGGGTGTTTT CAGGACTCAG CTGCCAAAGT 960
TTCTTGAAGC AGCTCTGCTC AAAGGCATAT GCTGGGCTCA CTTCTGAGGG AAATTTCCTT 1020
TTTGGGGAAG TTGAAGCAAA GGAATTTCCT GTGTGGGCAG ACAGAGCTTC CTGACTTGAA 1080
GGCTTCTTGG AAGGGAAACA GTTTCATAAT GAAATGACAA ATTAAAGACA TACCAGCCGG 1140
GTTCACTTCA AAACAGCTAT TGAGAGTGCA GGCAAAGCCC TATTATACTC CCTCACAGAA 1200
CAAAAATAAA TCCCATCCTG ACAGGTTTCT GTATGCCGGA TTATATCCGT CCCCCCACAC 1260
CTTTCTTCAC AGCCTTCTTC ATGCTTCCCT TCCTCCCACC CCCGCCATTA GCTGCCACCA 1320
GCTCCATCTT GAACAGCTCT CGAGAGCAGC CGGCAGCCAG GCCGGGAGCC TGTTTCTTGC 1380
TCCCTTGCTT TGTGGCTTTG CCCATCCCTG ACCTGCGTGG AGGCCTTATA GGTTATGTGA 1440
CAGCCCTATG CTGCCAAGAC ACAGAAATGA CCTCTTTCCT TCCCCTTTTG ACATAAAGCA 1500
ATGATTGAAG ACGTCTTCAG CAATGGGGTG GGGGCGGGCA GTCAGGGGAG AATGCAGCCA 1560
TTTCCTCAGG CCGGCCTTTA AAATCTTGAA GGCAGTAAAT GTAAGTGCTA TTCCGGTCTT 1620
GGGAGCTGGG TCTGAATTCT TTGCTTTGTT GAAGGAAATA GGGCTCTGTG CTGGGTGGAC 1680
GATATTCTTG TACCTGAACA TGTCATTTTC TTCAGTTCCA TCAGCCTGCA TGTGGTGCTT 1740
TGTTTTGTTT CTGAAATTGA CATGATGATG CCTTAGGAAC TAAATTTTTT TCTTTAATGG 1800
AACAGGCTAG GAGAAAGAAG 1820
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