Tag | Content |
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EnhancerAtlas ID | HS026-07448 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr12:11917970-11920250 |
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) |
Gata1 | MA0035.3 | chr12:11920162-11920173 | TCCTTATCTCT | + | 6.02 | 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 |
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| 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 |
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| 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I011761 | chr12 | 11914429 | 11925846 |
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Enhancer Sequence | ATAGTGTTGA GTTCCCCTTT GAGATCTGAC TGTGGTTAAA GCTTCACAAA TTTCAGAAAA 60 ACAGAATAAC TCACTAAAAT AAAAATTTAA AGCTACCCCA CAGAAAACAT CTACCACAAC 120 CCAAAACTTC AGGGTTTATA TATCCAGATT TTAGTGAACT ATATGACTCT CCCTAGTCCC 180 TTGCTCTGTC TCCTGGTAAA TACTGTCCCT TTCAGAGCCC TGGCACATAC ATAGTGTAAT 240 AAGATCAGAC CCCATCCCCC TACCATTCCA ATGCAATCTA ATTGCAAAGT GAAAATCCAG 300 GGCCGTCTTA GATCCTCATC TGTCTACGTC TCTCTTGGTC CCCACTGCTT GATACGCAGT 360 CTCAGGTTCA ATACCATTCT CTCTTTTTGT GCTTTAGGTC TCTGTATTGT TTCCTTTTCA 420 CCACTTTTTT TTTTTTAATG AAGTGATTTT AAATGGAAAA TTAAAAACTT AACTGTGAAT 480 CTGGCAGTTT CCTGCTAATG CCTCTTTGCT AAGAAGCTTC ATAAAATACT GTATCTTATT 540 CACTTCAGCA CAGCTGCTGT GGGCTCTCAC CACTTAACCA TTCACAATAT GTCTGAGAGA 600 TTAATTTTTG TAAGGCTGTG GTTTGAGATA TCTCCCCCTT CCTTGTTTTA CTTAAAATCC 660 TCAGTGGGAA AGCGTGCATG GGGAAAAAAA AAACCACCAC CACCCTGGAT AAAAGGTACT 720 TTGGTAACAT ACGTGCTTTA GGAACTATAA TTTGTCATTT TATTTTCTTG TGCCCTCTTC 780 ATTTGAAATG CTGCAGCCTT TCTGCCAGAA GTCTCAAGTT TGTGTATGAG ACTGAGGGGG 840 AAACGAGAGT AGGTACCTTG TGCTGAGACT GTCCTGGGAC AGTCCCGTGG TGGGTGTGAG 900 CGTCTGTGTG ATGCAGGTAT GCTTATTTCT TCATGAAAGC CGCAGGTACT GGTTGCCTCT 960 CGCAGGGTTA AAACTCTTGG CGGCTCACAG GAGGTGATGA AGAGCAAGGG CACGGGAGAA 1020 TGAAGAAGCA GGAGGAAGGT GTGGGCCAGG GTCGGTTTCG GTGGGGTCCC CACTTGCTGG 1080 GTGAAAGCTG AACTGTTTAT CCACACATCC CAGCAGCAGC AGAAAGCCAA GGGGTGTTTT 1140 CAGGACTCAG CTGCCAAAGT TTCTTGAAGC AGCTCTGCTC AAAGGCATAT GCTGGGCTCA 1200 CTTCTGAGGG AAATTTCCTT TTTGGGGAAG TTGAAGCAAA GGAATTTCCT GTGTGGGCAG 1260 ACAGAGCTTC CTGACTTGAA GGCTTCTTGG AAGGGAAACA GTTTCATAAT GAAATGACAA 1320 ATTAAAGACA TACCAGCCGG GTTCACTTCA AAACAGCTAT TGAGAGTGCA GGCAAAGCCC 1380 TATTATACTC CCTCACAGAA CAAAAATAAA TCCCATCCTG ACAGGTTTCT GTATGCCGGA 1440 TTATATCCGT CCCCCCACAC CTTTCTTCAC AGCCTTCTTC ATGCTTCCCT TCCTCCCACC 1500 CCCGCCATTA GCTGCCACCA GCTCCATCTT GAACAGCTCT CGAGAGCAGC CGGCAGCCAG 1560 GCCGGGAGCC TGTTTCTTGC TCCCTTGCTT TGTGGCTTTG CCCATCCCTG ACCTGCGTGG 1620 AGGCCTTATA GGTTATGTGA CAGCCCTATG CTGCCAAGAC ACAGAAATGA CCTCTTTCCT 1680 TCCCCTTTTG ACATAAAGCA ATGATTGAAG ACGTCTTCAG CAATGGGGTG GGGGCGGGCA 1740 GTCAGGGGAG AATGCAGCCA TTTCCTCAGG CCGGCCTTTA AAATCTTGAA GGCAGTAAAT 1800 GTAAGTGCTA TTCCGGTCTT GGGAGCTGGG TCTGAATTCT TTGCTTTGTT GAAGGAAATA 1860 GGGCTCTGTG CTGGGTGGAC GATATTCTTG TACCTGAACA TGTCATTTTC TTCAGTTCCA 1920 TCAGCCTGCA TGTGGTGCTT TGTTTTGTTT CTGAAATTGA CATGATGATG CCTTAGGAAC 1980 TAAATTTTTT TCTTTAATGG AACAGGCTAG GAGAAAGAAG GATGGCGGTA TCATTTGGGG 2040 CGTGAGAACA GTCATTATTA ATTAGGCTTA AGTTAATGAA ATAAAAAAGG CACAGGCTTT 2100 GAAATCAGTT GTCTAAATTT AAGGGCCAGC TCTAACAATA TACAACCAGC AATGTAACCT 2160 TGAACAAGTC ACTGAACCTC CCAGCCTCAG TTTCCTTATC TCTAAAATGG GTACAGTCAT 2220 ACCTTTTTCA CATTGTTGTG AGGAAATTAG ATTATGATTT CAGAGGCACT TTGTGAATTC 2280
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