Tag | Content |
---|
EnhancerAtlas ID | HS095-32094 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chrX:13018570-13021230 |
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 | POU2F2 | MA0507.1 | chrX:13018932-13018945 | ACATGCAAATAAA | - | 6.17 |
|
| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_11864 | chrX:13014939-13019645 | CD3 | SE_11864 | chrX:13020326-13020960 | CD3 | SE_14440 | chrX:13015562-13019221 | CD4_Memory_Primary_7pool | SE_15419 | chrX:13015762-13019379 | CD4_Memory_Primary_8pool | SE_15857 | chrX:13017095-13019036 | CD4_Naive_Primary_7pool | SE_16331 | chrX:13015966-13019167 | CD4_Naive_Primary_8pool | SE_16908 | chrX:13015988-13019310 | CD4p_CD225int_CD127p_Tmem | SE_17382 | chrX:13014282-13019833 | CD4p_CD25-_CD45RAp_Naive | SE_17382 | chrX:13020306-13022045 | CD4p_CD25-_CD45RAp_Naive | SE_17855 | chrX:13014461-13019788 | CD4p_CD25-_CD45ROp_Memory | SE_18339 | chrX:13013610-13021428 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19260 | chrX:13015862-13019546 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19260 | chrX:13019607-13020021 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_19260 | chrX:13020362-13020974 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20114 | chrX:13016105-13019457 | CD56 | SE_21967 | chrX:13017172-13019458 | CD8_Naive_8pool | SE_22410 | chrX:13014592-13019688 | CD8_primiary | SE_22410 | chrX:13020338-13021082 | CD8_primiary | SE_25447 | chrX:13014835-13020117 | DND41 | SE_28103 | chrX:13018293-13019272 | Fetal_Intestine | SE_28103 | chrX:13019309-13022035 | Fetal_Intestine | SE_29081 | chrX:13018232-13021800 | Fetal_Intestine_Large | SE_30940 | chrX:13015324-13019673 | Fetal_Thymus | SE_32462 | chrX:13015228-13027887 | GM12878 | SE_49904 | chrX:13014316-13019597 | RPMI-8402 | SE_50189 | chrX:13018095-13019076 | Sigmoid_Colon | SE_50189 | chrX:13019202-13020016 | Sigmoid_Colon | SE_52563 | chrX:13017463-13019092 | Small_Intestine | SE_58417 | chrX:12964783-13034394 | Ly1 | SE_58905 | chrX:12964721-13049077 | Ly3 | SE_62231 | chrX:12964510-13049336 | Tonsil | SE_66386 | chrX:13015915-13019351 | Jurkat |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chrX | 13020440 | 13020807 | chrX | 13018875 | 13019023 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH0XI012996 | chrX | 13014458 | 13022118 |
|
Enhancer Sequence | AGTGAAACCT TTTGTCATAT TCTGCACCAC TGATTTTTTC CAGACGAGCA GAAATGCCTG 60 CCTGTATATC CTTCTAAGGA CTGGCTAAGA AAGGGTGGAA AATAACAGGC AAGAAATGTA 120 TCTGTTTGAG TGTCTGTTCT TTGGTTTGGC TATGAAGTAA AACCCAAAAA CGACATTGAA 180 TTTGGCATTG GAAACTGCAG TGCCATTGTT GCTTTGGGAC TGGCTTAACA AGCCCACAAT 240 ATTCTAGAAG CATGTGCCCG TCCCAGGAGC CGACTCAGCC ATTTCTCAAA CATGAAGAGG 300 ACTGGGCCGT GCAGTCCTGT TTCCTCTTCC TGATCTTTGT AGTAGTTACA AGCTGAACAG 360 AAACATGCAA ATAAAAATCG AGAACCCTAA AGAGTAAGAA AATCATTTCC AGAAAGACTG 420 ATAATAAATT TCAAGCCATC AGCTCAAATA TCACTGATTT AAGTGCATTT GTTCCAGCTC 480 TTTTATAGAA TGTGAGGTTA AATACACAAA CTTGATATTA GAGTTGTCCC TGTACTAATT 540 CCCGCATGCG ATTCTTTTAA AAAGAAAAAT AAAATAGAAT GATTTTTAAA AATCTCATCT 600 AGAATGAGAA AACATAAAGT GCTTTTGGCT TTCCTTTCCC TGATTTTGAA GGGCTTTTTT 660 TTCCGCTTTT CCTTTACTTC CCTACCTTAA AGATGTTTAA ATTTAAGCCA GGTGTGAGCT 720 CTGAGAGAGA TCGAAGCTGC ATTTTATTTA CCTTTGTAGC TCAGACAACC AGAAATGGTA 780 GCGTTAGTAT TTGTGGAATG AGTCTTCACC TGACTTATCC TGAAGGGATG CATCTTCTAC 840 TTAGGATAAT GTTAGATTTG AATTTTACAA GATCCTGAGT CAGTAGTCTG TCATCCAGGC 900 TGCAGTGCAG TGGCACAATC ATGGCTCACT GCAGCCTGGA CCTCCCAGGC TCAAGTGATC 960 CTCCTACCTC AGCCTCCCAA GTAGCTGGGA CTATACGTGT GCACCACCAT GCTCGGCTAA 1020 TTTTTACATT TTTTGTAGAG AACAGGTCTC ACTACGTTGC TCAGACTGAT CTGGAACCCC 1080 TGGCTTCAAG TGACCCTCTC ACCTCAGCCT CCCAAAGCGC TGGGATTACA GGTATGAGCC 1140 ACTGCACCCC ACCATTATCA TTATTTTAGA GTGTACTCCT ACATATAGAT ATAAAGTTAA 1200 GTGTAAAACA GCCTCACGCA GGTCCTTCAG GAGGTATCCA GAAGAAGGCA TTGTTATCAT 1260 AGGAGATGAC AGCTCCATGC CTGTTACTTC CCCTGAGGAC CTTCCAGTGG GACAAGCTGT 1320 GGAGGTGGAA GACAGTGAGA TTGACAATCC TGAGCCTGTG TAGGCCTAGG CTAATGTCTG 1380 TGTTTGTGTA AAAACACACA CAAAAATAAA ATAAAAAGTT TGAAAATAGA AAAAAGTTTA 1440 CAGAATAAGG ATATAAAGAA AGAAAACATT TCTGTACAGC TGTACAATGT ATATTTTAAG 1500 CTGTTATTAC AAAAGAGTCA AAAAGCTAAA AAAATTCGAA GGTGTATAAA GTAAAAACGT 1560 TACAGTAAGC TAAGGTTAAT TTATTATTGA AGAAAGAAAA ATATTTTAAA CATAAATTTA 1620 ATGTAGCCTA AGTGTACAGT GTTTATAAAG TCTACTGTAG TATACAGTCA TGCCCTGTGC 1680 CTTCACATTC ACTCACCACT CACTGACTCA CCCAGAGCAA CTTCCAGTTT TGCAAGCTCC 1740 ATTTGTGGTA AGTGCCCTAT ACAGGTGAAC CATTTTTTAT CTTTTATACC ATATATTTAC 1800 TATACTTTTT CTATGTTTAG ATATACAAAT ACTCACCATT GTATTACAGT TGCCTACAGT 1860 ATTCAGTACA GGAACATGCT ATACAGGTTT GTAGACTAGG AGCAATAGGT TATACCATCT 1920 AGACTAGGTG TGCAGGAGGC TACACCAACT AGGTGTGTGT AAGTACCTCT ATGATCGAAC 1980 AATGATGAAA TCACCAAACG ATGCATTGCT CAGAACATAG CCCCATTGTT AAGTGATGTG 2040 TGACTATAAT TACACTACTG GGATTACATT TGGGAGAAGT AAGGTCTTCC TTTCTCTTTT 2100 TATGAGTTGG AAGATGTATT GAGAAAATCT GCCTTCAGCT GCTATAGTGG TGAGGTGGTG 2160 GTAGTTCTCT CTTGCTTCCT GTTAATCATT TACATTTATA TGGCCTATTA CAACAAAACA 2220 TTTCAAAGAA CCTCATAAAC GTGAGGATTG ATTCAATTAA ACTGTACTTC TGGTCTCTGG 2280 GATGAATATG ACAATGTTTT GTTCATCTCA GAACTGGAAA ATTAAGGCCC AGAAGTTGTA 2340 AAGATATTTC TCATTCCAAA TTCTGCATAT ATATATATTA TATGAATAAA TAATTCAAGA 2400 GAGTGAGGAA AAATCATATT TTTTTCTCCT TTGAGCTGGA AACAAAAACC CTTTGTACAG 2460 ATTTTGATGA TTCTTACTTC CTCCAAACCT TAGCTTTATT CATATGTTCT GCAAACTAAA 2520 CCACCATTAT GAAACCAACT GAAACTGTGA TCACAGGAGG CCATAAATAA ATTAGCTAAA 2580 GAATTAAAAT CCTCCTGGTC AGGGATTAAG CCTTTTATGA TCTTTCTCCT CTATGAAAAT 2640 ACCTTAATCT CTCCTCCTCT 2660
|