Tag | Content |
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EnhancerAtlas ID | HS113-03120 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:202014740-202017310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr1:202015499-202015511 | CTCTGTTTACAT | - | 6.32 | FOXP2 | MA0593.1 | chr1:202015500-202015511 | TCTGTTTACAT | - | 6.02 | IRF2 | MA0051.1 | chr1:202014977-202014995 | GGAAAATGAAACCTAAAG | + | 6.67 | Znf423 | MA0116.1 | chr1:202015407-202015422 | GCCCCCCTGGGGTGT | - | 6.21 | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | + | 6.36 | Znf423 | MA0116.1 | chr1:202015965-202015980 | GGCACCCTGGGTGGC | - | 6.66 |
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| Number of super-enhancer constituents: 21 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:202014631-202017594 | Colon_Crypt_1 | SE_23723 | chr1:202014745-202017484 | Colon_Crypt_2 | SE_24689 | chr1:202013412-202017599 | Colon_Crypt_3 | SE_25977 | chr1:202013680-202018944 | Duodenum_Smooth_Muscle | SE_26730 | chr1:202014480-202017654 | Esophagus | SE_27624 | chr1:202013379-202018834 | Fetal_Intestine | SE_28545 | chr1:202011166-202018857 | Fetal_Intestine_Large | SE_31432 | chr1:202014570-202017653 | Gastric | SE_33417 | chr1:202013470-202017710 | H2171 | SE_33792 | chr1:202014660-202017539 | HCC1954 | SE_34304 | chr1:202014463-202017386 | HCT-116 | SE_34741 | chr1:202015302-202017356 | HeLa | SE_41626 | chr1:202014836-202016985 | LNCaP | SE_43434 | chr1:202014625-202017551 | MCF-7 | SE_50066 | chr1:202013466-202017590 | Sigmoid_Colon | SE_52354 | chr1:202013521-202017654 | Small_Intestine | SE_56834 | chr1:202014865-202017504 | VACO_400 | SE_57376 | chr1:202014892-202016968 | VACO_503 | SE_57945 | chr1:202014917-202016359 | VACO_9m | SE_57945 | chr1:202016368-202017040 | VACO_9m | SE_65333 | chr1:202014451-202017286 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 202015600 | 202017009 | chr1 | 202016172 | 202016526 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I202042 | chr1 | 202011209 | 202018712 |
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Enhancer Sequence | TTCGGCTTCC CAAAGTGCTG GGATTACAGG TGTGAGCCAC TGCGCCTGGC CAACTGCATG 60 GAGTTTTTAA GATTTCCTAT GGCCCAAGTA CTCATAAGCA TCCTGCATGG ATTAACCCTG 120 AGAGGCAGGT GGTATTATTA TTCTCACTCT ACCTGGGTTC CCACCTGATA ATTGGTGAGG 180 CCCTTTCAAA TGTCCTTTGG CCTTCTATCC CCTGCCTTCT CTTGACTCCT TGAAGTGGGA 240 AAATGAAACC TAAAGTGCCT CCCTCCCCAG AGTGGGCCAT GTGGCGAACT CTATCCAATG 300 TCTCAGCACC TGCCACTCTC TAGTTGCATC CTGGCCATAG GCTGAATGGG TAGGGAGTTC 360 TCTGAGGCTG AGACCATGCT GTGAGGGAGG ATAGGCGGGC CAGGGACAGT GCCAGCAACA 420 GGGACCAGGG AGTGGTGGGA AGGTAAAATA AAGGCAGAGG AAACTTCTCC CAATTGAGGC 480 ACACCTACCC AAGGCCTCTG CCCCTACCCA GACTCCTGAC TTTGACCTGC CTAAAATAAA 540 TCCGGGGTCT GCAAATGGCC TGGAGGCTGC AAATGGCCTG AAGGCTAGTG GTTGGAGGGC 600 AAATAAAGGC AACTCATGGC ACTGCATGCT GCCCCTTGGT GGGCAGGTCC CAGGTCCCAG 660 GGTACCAGCC CCCCTGGGGT GTGATGTGGG CAGCCTCTGA GCTAAGTGAG GTGCAAACAA 720 GAAACCTGGG TTGCCTTTGC CCTCTGTCCG CCCCTTGTCC TCTGTTTACA TCCTCCCTTC 780 CCGTAAATGA GTTGGGTGCT GGGCCCCACT GGCCCTGATC CAGACACACC TGTAGGACAG 840 GTTGGGCAGA GCTCTTGGGG GTGGAGAGCG GGTGGCAGTA CTGGCAGGTG TTTCAGGCCC 900 TTGGGGAGCA AGCTCTGTTC CTTTCCATGG CAGTGCTGCT GCCAGGCTCT TGCTGCCTTG 960 GGCCAGGAAT TCTTGGCCAA CTCCAAAAGG ATGGGATGGC TCTAGGGGGG GCTACCTTGC 1020 CCAAGGAGTG CCAGGAAGTT GTGTTCAAGC CCTCAGAGGC AAGAGGACCA AAGGCTCTTT 1080 ATCTTCAGTG GGCATTTCCC AGCAGAAATC TGAGGTCTAG AGCGAGACAG AGTAGAATTG 1140 ACAATAAGAT CCACACTTGA GCTGCTAGCT GCCTTGATGG GAGACCCCAC TGTAACAAGA 1200 TGTCCAGGAG GAGGTGGCGG TACTGGGCAC CCTGGGTGGC TCTGCCTCTC TCTGGACTTT 1260 GTTCTGCAGT CAGGTCAGTT GAGGAAGCAA GAGTGAACCT GGAGTTTGGG TTTCTGGAAG 1320 GAGCAAGGGG GAAAGGCAGA CTTGGGCAAG GGACATAGGT GTCAGATGAG GCAAGTCTGA 1380 GTCAGAAGGC AGAGCCTGTG TCCCAGAGGA AGAGAAACAC CAGTGTCCAG CCTCCAGGCC 1440 ACTTGCAGCC CCCAGATTTA TTTTAGGCAG GTCAAAGTCA GGAGTCTGGG TAGGGGCAGA 1500 GGCCTTGGGT GGGTGTGTCT CAACTCAGAG AAGTTTCCTT TGCCACCAGA GGATTAACTG 1560 ACCAAGTTTA CCTAAGATGT GTTTTCCACC TGATCTCTTC TGTCTCTCTC AACAACAATG 1620 ATGACTGTGT ACTCAGTCAA CAAATATGTA GTAACTGCTT ACTATGTGCC CAGCCCTTTG 1680 CTGGGTGCTT AGATCACAGC TGTGTTCATT GGTGACTTTA CCAATCCATG GCATCATCTC 1740 GGTGGGGCAC TGTCCTGGTC AGCTCCTTCT CCCATTCCCT CCATCACTCC TCCACCCTCA 1800 CCTGCAGCTC CTGCATCTCT TGACTCTCAT CAAATGATCT TGCTGTCTTC TTCACGGGAA 1860 GGCCATGACC TCAAACAGGA AATCCTTCAG TTTCCCACCC TGCTGAATCT GTACCACCTT 1920 CCCTCCAGAG GAGTAGAAGA GGTGTCAACC CTGCCCCCGT GCTGGCGGTC CCAGTCCTGC 1980 TCAGCTTCTC TGGACAGGAG ATTAGCACAC AGAGGCTCAG CTCTAAGACC ACCTAGAGGC 2040 CTGCTTTAGG GGGTCCTGCT GAGTAAGGCA GAGGCTCAGG GTGGCCACAG TGGAGAACTG 2100 CTGGCTTAGC CTGCTTCCTG CATTGTGCCT GAGATGCCTG TGGCAAAGCT TTGCAGTCCC 2160 CACACCTGAT TCTGTATGTC CTGGGACACA ATGACTTGGA TTTCATCTTT TTTTTGTTTT 2220 TTCAAGCCAA AAATTAGGAT TCAGTTTATT CCAACATTGA ATGTATCAGG AAAACCAAAG 2280 ATAAAGTGAC AGAGGTACAT TAGGCACACT GTATACAGAT TTCATCTTTA CTTGACCTTT 2340 GCCAAAGAAC TATGCATATT CTGGTGATGG TGGTTTTCTT CAACAGATCT TTACGGGGAA 2400 GGCCCTCTCA TTTCCTCCAC ACCTTTCCTC TAGTGAAAGC GTTCTCAACC TCCAAGGAGT 2460 GTTGGGATTG TCTCCCCAGG TCATATCATC TGTCATCCAT ATGGGCTGTT AGCTCTGCGA 2520 TTTTTGTTCT CAGTCCCCAG GCTGTCTCTC AGCTCTAGAA GGAATTGTTC 2570
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