Tag | Content |
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EnhancerAtlas ID | HS165-03041 |
Organism | Homo sapiens |
Tissue/cell | Ramos |
Coordinate | chr12:11917760-11919990 |
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) |
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: 24 | ID | Coordinate | Tissue/cell |
SE_01754 | chr12:11916394-11918023 | Aorta | 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 | TATTGTATCA TTTAACCCTC TAGGCAGTCC TGTGAACTGG GTTTTATTAT CCTCATCTTA 60 CTGATGAAGA GTCAAACTTA AAGAGGAAAA GGAACTTGAC CAGAGTCACA GAGGTGGTAG 120 GTGGGAGACA GGTCCATCCA ATATACACCT TGCCTTCCAA TAGAAGCCAA AGCCCTATTG 180 CCTAATCTCT TCACTTTAAG AACATGAAGA ATAGTGTTGA GTTCCCCTTT GAGATCTGAC 240 TGTGGTTAAA GCTTCACAAA TTTCAGAAAA ACAGAATAAC TCACTAAAAT AAAAATTTAA 300 AGCTACCCCA CAGAAAACAT CTACCACAAC CCAAAACTTC AGGGTTTATA TATCCAGATT 360 TTAGTGAACT ATATGACTCT CCCTAGTCCC TTGCTCTGTC TCCTGGTAAA TACTGTCCCT 420 TTCAGAGCCC TGGCACATAC ATAGTGTAAT AAGATCAGAC CCCATCCCCC TACCATTCCA 480 ATGCAATCTA ATTGCAAAGT GAAAATCCAG GGCCGTCTTA GATCCTCATC TGTCTACGTC 540 TCTCTTGGTC CCCACTGCTT GATACGCAGT CTCAGGTTCA ATACCATTCT CTCTTTTTGT 600 GCTTTAGGTC TCTGTATTGT TTCCTTTTCA CCACTTTTTT TTTTTTAATG AAGTGATTTT 660 AAATGGAAAA TTAAAAACTT AACTGTGAAT CTGGCAGTTT CCTGCTAATG CCTCTTTGCT 720 AAGAAGCTTC ATAAAATACT GTATCTTATT CACTTCAGCA CAGCTGCTGT GGGCTCTCAC 780 CACTTAACCA TTCACAATAT GTCTGAGAGA TTAATTTTTG TAAGGCTGTG GTTTGAGATA 840 TCTCCCCCTT CCTTGTTTTA CTTAAAATCC TCAGTGGGAA AGCGTGCATG GGGAAAAAAA 900 AAACCACCAC CACCCTGGAT AAAAGGTACT TTGGTAACAT ACGTGCTTTA GGAACTATAA 960 TTTGTCATTT TATTTTCTTG TGCCCTCTTC ATTTGAAATG CTGCAGCCTT TCTGCCAGAA 1020 GTCTCAAGTT TGTGTATGAG ACTGAGGGGG AAACGAGAGT AGGTACCTTG TGCTGAGACT 1080 GTCCTGGGAC AGTCCCGTGG TGGGTGTGAG CGTCTGTGTG ATGCAGGTAT GCTTATTTCT 1140 TCATGAAAGC CGCAGGTACT GGTTGCCTCT CGCAGGGTTA AAACTCTTGG CGGCTCACAG 1200 GAGGTGATGA AGAGCAAGGG CACGGGAGAA TGAAGAAGCA GGAGGAAGGT GTGGGCCAGG 1260 GTCGGTTTCG GTGGGGTCCC CACTTGCTGG GTGAAAGCTG AACTGTTTAT CCACACATCC 1320 CAGCAGCAGC AGAAAGCCAA GGGGTGTTTT CAGGACTCAG CTGCCAAAGT TTCTTGAAGC 1380 AGCTCTGCTC AAAGGCATAT GCTGGGCTCA CTTCTGAGGG AAATTTCCTT TTTGGGGAAG 1440 TTGAAGCAAA GGAATTTCCT GTGTGGGCAG ACAGAGCTTC CTGACTTGAA GGCTTCTTGG 1500 AAGGGAAACA GTTTCATAAT GAAATGACAA ATTAAAGACA TACCAGCCGG GTTCACTTCA 1560 AAACAGCTAT TGAGAGTGCA GGCAAAGCCC TATTATACTC CCTCACAGAA CAAAAATAAA 1620 TCCCATCCTG ACAGGTTTCT GTATGCCGGA TTATATCCGT CCCCCCACAC CTTTCTTCAC 1680 AGCCTTCTTC ATGCTTCCCT TCCTCCCACC CCCGCCATTA GCTGCCACCA GCTCCATCTT 1740 GAACAGCTCT CGAGAGCAGC CGGCAGCCAG GCCGGGAGCC TGTTTCTTGC TCCCTTGCTT 1800 TGTGGCTTTG CCCATCCCTG ACCTGCGTGG AGGCCTTATA GGTTATGTGA CAGCCCTATG 1860 CTGCCAAGAC ACAGAAATGA CCTCTTTCCT TCCCCTTTTG ACATAAAGCA ATGATTGAAG 1920 ACGTCTTCAG CAATGGGGTG GGGGCGGGCA GTCAGGGGAG AATGCAGCCA TTTCCTCAGG 1980 CCGGCCTTTA AAATCTTGAA GGCAGTAAAT GTAAGTGCTA TTCCGGTCTT GGGAGCTGGG 2040 TCTGAATTCT TTGCTTTGTT GAAGGAAATA GGGCTCTGTG CTGGGTGGAC GATATTCTTG 2100 TACCTGAACA TGTCATTTTC TTCAGTTCCA TCAGCCTGCA TGTGGTGCTT TGTTTTGTTT 2160 CTGAAATTGA CATGATGATG CCTTAGGAAC TAAATTTTTT TCTTTAATGG AACAGGCTAG 2220 GAGAAAGAAG 2230
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