Tag | Content |
---|
EnhancerAtlas ID | HS044-03044 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr12:11918010-11920260 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 |
|
| 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 | GCTTCACAAA TTTCAGAAAA ACAGAATAAC TCACTAAAAT AAAAATTTAA AGCTACCCCA 60 CAGAAAACAT CTACCACAAC CCAAAACTTC AGGGTTTATA TATCCAGATT TTAGTGAACT 120 ATATGACTCT CCCTAGTCCC TTGCTCTGTC TCCTGGTAAA TACTGTCCCT TTCAGAGCCC 180 TGGCACATAC ATAGTGTAAT AAGATCAGAC CCCATCCCCC TACCATTCCA ATGCAATCTA 240 ATTGCAAAGT GAAAATCCAG GGCCGTCTTA GATCCTCATC TGTCTACGTC TCTCTTGGTC 300 CCCACTGCTT GATACGCAGT CTCAGGTTCA ATACCATTCT CTCTTTTTGT GCTTTAGGTC 360 TCTGTATTGT TTCCTTTTCA CCACTTTTTT TTTTTTAATG AAGTGATTTT AAATGGAAAA 420 TTAAAAACTT AACTGTGAAT CTGGCAGTTT CCTGCTAATG CCTCTTTGCT AAGAAGCTTC 480 ATAAAATACT GTATCTTATT CACTTCAGCA CAGCTGCTGT GGGCTCTCAC CACTTAACCA 540 TTCACAATAT GTCTGAGAGA TTAATTTTTG TAAGGCTGTG GTTTGAGATA TCTCCCCCTT 600 CCTTGTTTTA CTTAAAATCC TCAGTGGGAA AGCGTGCATG GGGAAAAAAA AAACCACCAC 660 CACCCTGGAT AAAAGGTACT TTGGTAACAT ACGTGCTTTA GGAACTATAA TTTGTCATTT 720 TATTTTCTTG TGCCCTCTTC ATTTGAAATG CTGCAGCCTT TCTGCCAGAA GTCTCAAGTT 780 TGTGTATGAG ACTGAGGGGG AAACGAGAGT AGGTACCTTG TGCTGAGACT GTCCTGGGAC 840 AGTCCCGTGG TGGGTGTGAG CGTCTGTGTG ATGCAGGTAT GCTTATTTCT TCATGAAAGC 900 CGCAGGTACT GGTTGCCTCT CGCAGGGTTA AAACTCTTGG CGGCTCACAG GAGGTGATGA 960 AGAGCAAGGG CACGGGAGAA TGAAGAAGCA GGAGGAAGGT GTGGGCCAGG GTCGGTTTCG 1020 GTGGGGTCCC CACTTGCTGG GTGAAAGCTG AACTGTTTAT CCACACATCC CAGCAGCAGC 1080 AGAAAGCCAA GGGGTGTTTT CAGGACTCAG CTGCCAAAGT TTCTTGAAGC AGCTCTGCTC 1140 AAAGGCATAT GCTGGGCTCA CTTCTGAGGG AAATTTCCTT TTTGGGGAAG TTGAAGCAAA 1200 GGAATTTCCT GTGTGGGCAG ACAGAGCTTC CTGACTTGAA GGCTTCTTGG AAGGGAAACA 1260 GTTTCATAAT GAAATGACAA ATTAAAGACA TACCAGCCGG GTTCACTTCA AAACAGCTAT 1320 TGAGAGTGCA GGCAAAGCCC TATTATACTC CCTCACAGAA CAAAAATAAA TCCCATCCTG 1380 ACAGGTTTCT GTATGCCGGA TTATATCCGT CCCCCCACAC CTTTCTTCAC AGCCTTCTTC 1440 ATGCTTCCCT TCCTCCCACC CCCGCCATTA GCTGCCACCA GCTCCATCTT GAACAGCTCT 1500 CGAGAGCAGC CGGCAGCCAG GCCGGGAGCC TGTTTCTTGC TCCCTTGCTT TGTGGCTTTG 1560 CCCATCCCTG ACCTGCGTGG AGGCCTTATA GGTTATGTGA CAGCCCTATG CTGCCAAGAC 1620 ACAGAAATGA CCTCTTTCCT TCCCCTTTTG ACATAAAGCA ATGATTGAAG ACGTCTTCAG 1680 CAATGGGGTG GGGGCGGGCA GTCAGGGGAG AATGCAGCCA TTTCCTCAGG CCGGCCTTTA 1740 AAATCTTGAA GGCAGTAAAT GTAAGTGCTA TTCCGGTCTT GGGAGCTGGG TCTGAATTCT 1800 TTGCTTTGTT GAAGGAAATA GGGCTCTGTG CTGGGTGGAC GATATTCTTG TACCTGAACA 1860 TGTCATTTTC TTCAGTTCCA TCAGCCTGCA TGTGGTGCTT TGTTTTGTTT CTGAAATTGA 1920 CATGATGATG CCTTAGGAAC TAAATTTTTT TCTTTAATGG AACAGGCTAG GAGAAAGAAG 1980 GATGGCGGTA TCATTTGGGG CGTGAGAACA GTCATTATTA ATTAGGCTTA AGTTAATGAA 2040 ATAAAAAAGG CACAGGCTTT GAAATCAGTT GTCTAAATTT AAGGGCCAGC TCTAACAATA 2100 TACAACCAGC AATGTAACCT TGAACAAGTC ACTGAACCTC CCAGCCTCAG TTTCCTTATC 2160 TCTAAAATGG GTACAGTCAT ACCTTTTTCA CATTGTTGTG AGGAAATTAG ATTATGATTT 2220 CAGAGGCACT TTGTGAATTC CTATAAGCCT 2250
|