Tag | Content |
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EnhancerAtlas ID | HS180-28229 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr2:197075760-197076880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Stat6 | MA0520.1 | chr2:197076092-197076107 | GTCTTCCACAGAAAT | + | 6.15 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_17651 | chr2:197074684-197079827 | CD4p_CD25-_CD45RAp_Naive | SE_18248 | chr2:197075268-197078680 | CD4p_CD25-_Il17-_PMAstim_Th | SE_25416 | chr2:197074644-197077240 | DND41 | SE_44074 | chr2:197075282-197076918 | MM1S | SE_58309 | chr2:197014096-197142249 | Ly1 | SE_59970 | chr2:197014195-197079563 | Ly4 | SE_62200 | chr2:197013935-197160826 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr2 | 197076200 | 197076795 | chr2 | 197075977 | 197076359 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I196210 | chr2 | 197075289 | 197077323 |
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Enhancer Sequence | AACTCTTACA ATTTATTTCT TAATTTCAGT TAGCATTTCA TTCATAATAA TCTCCAGACA 60 CAGCCATTTT CAAAAATTAA CGCTTTTCCC TTTGGCAATA ACCAACACAC CCCCATGACG 120 ATTGCAGCTC TCAGGTCCTC CGTCCCATCA CCCAACTTGG CAAGAACCTG GGGGATGAAC 180 ACAGAAACTC ACACCATGGT GGGAGACAGG ACTGCTCTGC AGTTTTCAGG CTGGCATCTT 240 AGCAGCGCAT TTTTTGGACT GTTTGAGAGC AATTGCCACA AAGTGAATGT ACTCTCTTTT 300 CATAAAGTCC ATCAGAGCAC CAGGGGTATG AAGTCTTCCA CAGAAATGCA AAATACAGAG 360 CTAACCACCG ACCGCGAAGC AGAGGAAGTG CAGTCATGTG CTCAGGCTGT AGGTCTCCAT 420 GGAGACACCC TTCTGTCTAC ATCCTTATTT ATCATCTGGG TCTCTAGTCA CTTCATAACC 480 ACAAGAGGAA AAAAGAGCCA TGGATTCAAC TTGCACTGGC TGCAGAGACA ACCATATATA 540 CTTTTATATA CTCCTTGACT CATACTGTGA GCAGCGCTAT CCACTGCTAC CGCAAAGTGA 600 GACTAGGAAA TCTGAGAAAA GAATGAGACT CACATTTGCC TGCTTGAAAA TTGAAAGGCC 660 CTCCATCATC CTTGTCTAGA AAGACTAAGA TTCTCTCCCT CATTGCTCCG GTTGCCAGGA 720 CTGCCCTCAT CCTTTACAGC CCCTCCAACC CTCCAGGGCA GAAACTCCCA TGCCCGACAC 780 AAGACCATGC CAGACTTCTT AGAGGATTCT TTTTTTTTCT TTTTGAGACA GAGTCTTGCT 840 CTGTCGCCCA GGCTGGAGTG CAGCATTGCC ATCTCGGCTC ACTGCAACCT CTGCCTCCTG 900 GGTTCAAGCG ATTCTCCTGC CTCCCGAGTA GCTGGGACTA TAGGCGTATG CCACCACGCC 960 CAGGTAATTT TTGTATTTTT AGTAGAGACA GGGTTTCACC ATGTTAGCCA GGCTGGTCTC 1020 AAACTCCTGA CCTCAGGCAA TCCGTCCGCC TTGGCCTCCC AAAGTGCTGG GATTACAGGT 1080 GTGAGCCACC ATGCCCAGCC AGGATTCATT TTTTAAGTAA 1120
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