| Tag | Content |
|---|
EnhancerAtlas ID | HS180-10719 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr12:11918090-11920030 |
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 | CCAAAACTTC AGGGTTTATA TATCCAGATT TTAGTGAACT ATATGACTCT CCCTAGTCCC 60
TTGCTCTGTC TCCTGGTAAA TACTGTCCCT TTCAGAGCCC TGGCACATAC ATAGTGTAAT 120
AAGATCAGAC CCCATCCCCC TACCATTCCA ATGCAATCTA ATTGCAAAGT GAAAATCCAG 180
GGCCGTCTTA GATCCTCATC TGTCTACGTC TCTCTTGGTC CCCACTGCTT GATACGCAGT 240
CTCAGGTTCA ATACCATTCT CTCTTTTTGT GCTTTAGGTC TCTGTATTGT TTCCTTTTCA 300
CCACTTTTTT TTTTTTAATG AAGTGATTTT AAATGGAAAA TTAAAAACTT AACTGTGAAT 360
CTGGCAGTTT CCTGCTAATG CCTCTTTGCT AAGAAGCTTC ATAAAATACT GTATCTTATT 420
CACTTCAGCA CAGCTGCTGT GGGCTCTCAC CACTTAACCA TTCACAATAT GTCTGAGAGA 480
TTAATTTTTG TAAGGCTGTG GTTTGAGATA TCTCCCCCTT CCTTGTTTTA CTTAAAATCC 540
TCAGTGGGAA AGCGTGCATG GGGAAAAAAA AAACCACCAC CACCCTGGAT AAAAGGTACT 600
TTGGTAACAT ACGTGCTTTA GGAACTATAA TTTGTCATTT TATTTTCTTG TGCCCTCTTC 660
ATTTGAAATG CTGCAGCCTT TCTGCCAGAA GTCTCAAGTT TGTGTATGAG ACTGAGGGGG 720
AAACGAGAGT AGGTACCTTG TGCTGAGACT GTCCTGGGAC AGTCCCGTGG TGGGTGTGAG 780
CGTCTGTGTG ATGCAGGTAT GCTTATTTCT TCATGAAAGC CGCAGGTACT GGTTGCCTCT 840
CGCAGGGTTA AAACTCTTGG CGGCTCACAG GAGGTGATGA AGAGCAAGGG CACGGGAGAA 900
TGAAGAAGCA GGAGGAAGGT GTGGGCCAGG GTCGGTTTCG GTGGGGTCCC CACTTGCTGG 960
GTGAAAGCTG AACTGTTTAT CCACACATCC CAGCAGCAGC AGAAAGCCAA GGGGTGTTTT 1020
CAGGACTCAG CTGCCAAAGT TTCTTGAAGC AGCTCTGCTC AAAGGCATAT GCTGGGCTCA 1080
CTTCTGAGGG AAATTTCCTT TTTGGGGAAG TTGAAGCAAA GGAATTTCCT GTGTGGGCAG 1140
ACAGAGCTTC CTGACTTGAA GGCTTCTTGG AAGGGAAACA GTTTCATAAT GAAATGACAA 1200
ATTAAAGACA TACCAGCCGG GTTCACTTCA AAACAGCTAT TGAGAGTGCA GGCAAAGCCC 1260
TATTATACTC CCTCACAGAA CAAAAATAAA TCCCATCCTG ACAGGTTTCT GTATGCCGGA 1320
TTATATCCGT CCCCCCACAC CTTTCTTCAC AGCCTTCTTC ATGCTTCCCT TCCTCCCACC 1380
CCCGCCATTA GCTGCCACCA GCTCCATCTT GAACAGCTCT CGAGAGCAGC CGGCAGCCAG 1440
GCCGGGAGCC TGTTTCTTGC TCCCTTGCTT TGTGGCTTTG CCCATCCCTG ACCTGCGTGG 1500
AGGCCTTATA GGTTATGTGA CAGCCCTATG CTGCCAAGAC ACAGAAATGA CCTCTTTCCT 1560
TCCCCTTTTG ACATAAAGCA ATGATTGAAG ACGTCTTCAG CAATGGGGTG GGGGCGGGCA 1620
GTCAGGGGAG AATGCAGCCA TTTCCTCAGG CCGGCCTTTA AAATCTTGAA GGCAGTAAAT 1680
GTAAGTGCTA TTCCGGTCTT GGGAGCTGGG TCTGAATTCT TTGCTTTGTT GAAGGAAATA 1740
GGGCTCTGTG CTGGGTGGAC GATATTCTTG TACCTGAACA TGTCATTTTC TTCAGTTCCA 1800
TCAGCCTGCA TGTGGTGCTT TGTTTTGTTT CTGAAATTGA CATGATGATG CCTTAGGAAC 1860
TAAATTTTTT TCTTTAATGG AACAGGCTAG GAGAAAGAAG GATGGCGGTA TCATTTGGGG 1920
CGTGAGAACA GTCATTATTA 1940
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