Tag | Content |
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EnhancerAtlas ID | HS053-41743 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chrX:13020200-13020920 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chrX:13020749-13020764 | TGTTAATCATTTACA | + | 6.29 | HNF1A | MA0046.2 | chrX:13020749-13020764 | TGTTAATCATTTACA | - | 6.79 | HNF1B | MA0153.2 | chrX:13020750-13020763 | GTTAATCATTTAC | + | 6.39 | HNF1B | MA0153.2 | chrX:13020750-13020763 | GTTAATCATTTAC | - | 6.87 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_11864 | chrX:13020326-13020960 | CD3 | SE_17382 | chrX:13020306-13022045 | CD4p_CD25-_CD45RAp_Naive | SE_18339 | chrX:13013610-13021428 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19260 | chrX:13020362-13020974 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_22410 | chrX:13020338-13021082 | CD8_primiary | SE_28103 | chrX:13019309-13022035 | Fetal_Intestine | SE_29081 | chrX:13018232-13021800 | Fetal_Intestine_Large | SE_32462 | chrX:13015228-13027887 | GM12878 | SE_58417 | chrX:12964783-13034394 | Ly1 | SE_58905 | chrX:12964721-13049077 | Ly3 | SE_62231 | chrX:12964510-13049336 | Tonsil |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH0XI012996 | chrX | 13014458 | 13022118 |
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Enhancer Sequence | AGTGTACAGT GTTTATAAAG TCTACTGTAG TATACAGTCA TGCCCTGTGC CTTCACATTC 60 ACTCACCACT CACTGACTCA CCCAGAGCAA CTTCCAGTTT TGCAAGCTCC ATTTGTGGTA 120 AGTGCCCTAT ACAGGTGAAC CATTTTTTAT CTTTTATACC ATATATTTAC TATACTTTTT 180 CTATGTTTAG ATATACAAAT ACTCACCATT GTATTACAGT TGCCTACAGT ATTCAGTACA 240 GGAACATGCT ATACAGGTTT GTAGACTAGG AGCAATAGGT TATACCATCT AGACTAGGTG 300 TGCAGGAGGC TACACCAACT AGGTGTGTGT AAGTACCTCT ATGATCGAAC AATGATGAAA 360 TCACCAAACG ATGCATTGCT CAGAACATAG CCCCATTGTT AAGTGATGTG TGACTATAAT 420 TACACTACTG GGATTACATT TGGGAGAAGT AAGGTCTTCC TTTCTCTTTT TATGAGTTGG 480 AAGATGTATT GAGAAAATCT GCCTTCAGCT GCTATAGTGG TGAGGTGGTG GTAGTTCTCT 540 CTTGCTTCCT GTTAATCATT TACATTTATA TGGCCTATTA CAACAAAACA TTTCAAAGAA 600 CCTCATAAAC GTGAGGATTG ATTCAATTAA ACTGTACTTC TGGTCTCTGG GATGAATATG 660 ACAATGTTTT GTTCATCTCA GAACTGGAAA ATTAAGGCCC AGAAGTTGTA AAGATATTTC 720
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