Tag | Content |
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EnhancerAtlas ID | HS180-04621 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr1:223908490-223909630 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT3 | MA0144.2 | chr1:223908784-223908795 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223891886-223912166 | Adipose_Nuclei | SE_01908 | chr1:223908439-223909567 | Aorta | SE_02306 | chr1:223908173-223909671 | Astrocytes | SE_09681 | chr1:223908083-223912580 | CD14 | SE_19702 | chr1:223908760-223910194 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_23408 | chr1:223908424-223909691 | Colon_Crypt_1 | SE_24051 | chr1:223908439-223908768 | Colon_Crypt_2 | SE_24051 | chr1:223908866-223909579 | Colon_Crypt_2 | SE_25230 | chr1:223908229-223909855 | Colon_Crypt_3 | SE_26209 | chr1:223907335-223910192 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223908287-223909800 | Esophagus | SE_31491 | chr1:223907108-223909701 | Gastric | SE_33950 | chr1:223907117-223909775 | HCC1954 | SE_34979 | chr1:223908435-223909798 | HeLa | SE_36294 | chr1:223908325-223909765 | HMEC | SE_37129 | chr1:223899390-223911201 | HSMMtube | SE_42269 | chr1:223907334-223909767 | Lung | SE_44904 | chr1:223907251-223909858 | NHLF | SE_45872 | chr1:223899383-223910101 | Osteoblasts | SE_49408 | chr1:223908481-223909631 | Right_Atrium | SE_50365 | chr1:223907302-223909908 | Sigmoid_Colon | SE_51879 | chr1:223908189-223908855 | Skeletal_Muscle_Myoblast | SE_51879 | chr1:223908921-223909593 | Skeletal_Muscle_Myoblast | SE_53249 | chr1:223908284-223909766 | Small_Intestine | SE_55958 | chr1:223908900-223910047 | u87 | SE_63671 | chr1:223908189-223909737 | HSMM | SE_64794 | chr1:223908347-223911615 | NHEK | SE_65644 | chr1:223908923-223909708 | Pancreatic_islets | SE_67677 | chr1:223908900-223910047 | u87 | SE_68376 | chr1:223892363-223922876 | TC32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | CGGGAGAGTA AGTGTAAAGC CACACAGCTA GTAATTGCCA AAGGATTGAA CCCTGGTCTG 60 ATTTTGAATC CTACACTCTT CCTAACCCAT GCTCCCTCCA ATTTGCCATA GTGCTGTGCT 120 GAGGAACCAT TCTCAGCAAA ATTCATCTTC TCTACCTGCG CTTTCTACCC TGAGCCTTAC 180 TCAGTTCCCC CAGGGAACTT GGGCAGGTGA CATTCTTAGA CTTGTGCACT TTGCAACGCC 240 CTGCCCTGTT TACTGTGCTG CCCAGCAATG TTTAATCCAC AAACACCCAC GCTCCTTCCC 300 AGAAGGCTCA GCTTCCAAGC TTCACCAAAG TCATTTAAAC CATGTTTACA GAGCTGCTCT 360 CACCAAGAGC CATCTCCATT GCAGAATATA GTTGTGTAAG AATTGATTCA GCAGAGAAAA 420 ATCTGCCCTT CTGGAGGAAG GGCTGGAGAC CCAGCTGGAG CCTCCACTGG CTGACCCTGC 480 AGCTAAATAT GGCTCTGAAA TCGTGGGGTA ATAACCACAT TCTTACAGGT GCTTGCCACT 540 TGAAATGGCT CCCAAGGACC CAGGAAACTC CAAGGCTGAG CTGCTCCTAC CTCTGATGCT 600 TTACTTTGCA CTGGGTCACC ACTGAGCTTT CCCCACAGCC TCACAGCTCA CGGATGAAGG 660 CAGCTACCCC AGCCAGGAAG GCATAGGTCA CCTTGCAGGC CTCTGATTTC CTGGGGTAGA 720 GCCCAAGGCT GCCAAGGCTG TTGAAACAGC ACACCCCCAT TTCATTGTAA CCCAGCAAAT 780 GTTCCCTGGG CCCCTCAGAG GTGGGTCAAC CTGCCTCCTT CTCAAGATGT CACATGGACC 840 CCCAGAGCAC CCACTGGGAG GTGTTTAGCT ACAGGGTGCC CCACCCCACA GCCTAGCTCA 900 GCAGAGAGTG GGGAAGGGAC AAGACCAATG GGAAAGGCAA GCCAGATGGG GAATTTTCCA 960 GTCCTGTTCC TTCTACCACT CATTAGCCAC TTATTTGGAC CCAACCCCTC TGAGCCTCAG 1020 TTTCTTCTTC TGTGAAATGG GAATAATGAT AAGGATCCCT TCCCAGGGCT GTGGAGAAAA 1080 GTGAGATTTA TACAGGCAAA CACACTTGGC ACACTATAGA ATCCCAGACA AATTCAAGGG 1140
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