Tag | Content |
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EnhancerAtlas ID | HS101-28721 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr22:29217420-29219980 |
Target genes | Number: 14 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr22:29218261-29218273 | GTTTGTTTGTTT | + | 6.32 | Foxd3 | MA0041.1 | chr22:29218265-29218277 | GTTTGTTTGTTT | + | 6.32 | GFI1 | MA0038.2 | chr22:29218614-29218626 | TGCAGTGATTTT | - | 6.11 | ZNF263 | MA0528.1 | chr22:29218582-29218603 | TTTTCCTTCTCCTTCTCCTCT | - | 7.15 |
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| Number of super-enhancer constituents: 27 | ID | Coordinate | Tissue/cell |
SE_13369 | chr22:29218532-29220102 | CD34_Primary_RO01536 | SE_14087 | chr22:29218571-29219697 | CD34_Primary_RO01549 | SE_14873 | chr22:29218340-29220196 | CD4_Memory_Primary_7pool | SE_18901 | chr22:29218464-29220036 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19461 | chr22:29218813-29219666 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_21193 | chr22:29218725-29219761 | CD8_Memory_7pool | SE_23503 | chr22:29216824-29217924 | Colon_Crypt_1 | SE_23503 | chr22:29218482-29218939 | Colon_Crypt_1 | SE_23503 | chr22:29219047-29219903 | Colon_Crypt_1 | SE_25378 | chr22:29203596-29221521 | DND41 | SE_28436 | chr22:29218500-29219878 | Fetal_Intestine | SE_29251 | chr22:29218848-29219910 | Fetal_Intestine_Large | SE_31018 | chr22:29216756-29221331 | Fetal_Thymus | SE_31638 | chr22:29213521-29220117 | Gastric | SE_33938 | chr22:29217571-29220537 | HCC1954 | SE_35317 | chr22:29218400-29219910 | HepG2 | SE_43412 | chr22:29216782-29219958 | MCF-7 | SE_43527 | chr22:29212224-29222080 | MM1S | SE_50644 | chr22:29216767-29219958 | Sigmoid_Colon | SE_52811 | chr22:29216768-29218293 | Small_Intestine | SE_52811 | chr22:29218440-29219724 | Small_Intestine | SE_55644 | chr22:29217457-29218303 | Thymus | SE_55644 | chr22:29218481-29220015 | Thymus | SE_62966 | chr22:29186510-29220159 | Tonsil | SE_66754 | chr22:29218445-29218868 | Jurkat | SE_66754 | chr22:29219009-29219860 | Jurkat | SE_67157 | chr22:29212224-29222080 | MM1S |
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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 |
GH22I028807 | chr22 | 29203221 | 29221297 |
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Enhancer Sequence | TGTGATCATG GCTCACTGCA GCCTCCACCT CTCAGGCTCA TATGATCCTC CTGCCTCAGC 60 CTCCCAAGTA GCTGGGACAA CAGACATGTA CCACCATGCC CAGCTAATAG GGACTGTATC 120 TTATGTATGA ACCTTTGTAA CTCTCAAGCC ACTTGATAGC CCTCAGTAAC TATTATTGGC 180 CAAATTTGTC CTTTTTGGCA GAGCACCTGG CAGGGACTCA GTACATCCCT AATCAGTTGC 240 TCATCTGAGG CACAGAAAGG TTAAAAGTGA TGCAGCCAGG ACCTGCTGGC AAATCCCCAT 300 GGCTCCAGCA CCAGGCCTGT CTGGCTCCTG AACCTCTGAC CTACTGCTGC TCATCCATAT 360 CTATCTCCTG AGACCTCGAG ACATGAATCC ACCTTGGGTA ACCTGTAAAG ACTTATTTGC 420 CTAAAACCTG CCCAGGAGTC TTAATGTCCC CATCCCGTTT TAATAGATGA ACACTTTGCT 480 TTTGGAAACT TTCTGTTCCT TGGATATTGA TGGTCATATT GCTTCTGGAA TCATTACAGT 540 GTGCCTTCAG CCAAAAGCAG AACTGGAAAC ATCCTAAGTG GGCCGGTAAC GAGGCTAGCT 600 CTGTCGACTA GTTCAAGACC CCTGAGCGCT TTGGGCCTGA GGTTCCTCAG CTTCCAAGTG 660 AAAGGCTTCG ACTTGGCATT CTAAGAGACA ATCTCTGTGA CCATCAGTTT CCTCATCTGT 720 AAAACTGGCA TCATGATAAC TTTGAAGGTA ATTGTGAAGA TTAAAGGGAG TCATGCATGT 780 AAACCACCTT GCATAGTCCC TTGTGGGAGT TCTTGGTTTT TTGTTTTTTT GGGGTTTTTT 840 GGTTTGTTTG TTTGTTTTGA AACAGAGTCT TGCTCTGTCG CCCAGACTGG AGTGCAGTGG 900 TGCAATCTCG GCTCACTGCA GCCTCCACCT CCCTGATTCA AATGATTCTT GCACCTCAGC 960 CTCCCGAGTA GCTGGGATTA CAGGCGCCTG CCACCATGCC CAGCTAATTT TTGTATTTTT 1020 AGTAGAGACA GAGTTTCGCC CTGTTGGCCA GGCTGGTCTC AAACTCCTGG CCTCAAGTGA 1080 TCCACCTGCC TCGGCCTCAC AAAGTGCTAG GATTACAGGT GTAAGTCACC TTGCCCGCCC 1140 GGGAGTTCAT TTATTAGCTT GTTTTTCCTT CTCCTTCTCC TCTTAAGTCT AAACTGCAGT 1200 GATTTTATGA TTCCACTTTT CGAGTCAGTG CCCCAGATGG TTTGCTCATT CATTCATTCA 1260 CCCCAAAAAA TGTTTATTGT TCACCTACTA TGTGGCAAGC ATCACACTAG GTACTGGGTG 1320 CTAAGCATAT GGTGGTGGGC AAGAACCTCT CTAGAAAACA TCAGAAATTG TCCAGCAATC 1380 CCCAGCAATG CAAAGAAAGA CACAGCAAAA AAATGCATGA TCAAATGCAT CCAGAAGTCT 1440 GAAATTATAA CTTTTATAAT TGTTTCAAGT GAATTCTGAG TAGATGCTAC TTAGCAGGTG 1500 GCCACAGTTC TCCCCAGTAG CTGCTGTTCC ACTTAAGACA CCTGCTGCTG TTTCCAGGAT 1560 GCTAACATTT ACTTTGGTCT TTATGTCAAT GTCATTTGCA GAGAGAGCCA GCTGTGTGGC 1620 TTTTTCTCTT TCAACATTGC CACTGAATTG TGCTTTGTTG ACAGAAATTA AACACTGCTC 1680 ACGTAGATAG CATCAGGGCA GCCTTCAAGA CTGGTTTGAA CAGGAACCTT CTGCCCAAGA 1740 TGAAGAGTAG ACTCTATCTT GGGGTTAGGA ATGTTTTCCT TCTTTGTGGC TTGATCATCT 1800 GGCCAAATTT TACTTTACCT AGTGCTGCTT TTGTTCCCCT GGCTTTCCTT CCTTGGAGCC 1860 CTTTTAAAAT AATCCTTCTC TGCTTGTGGG ATTTTACCAG ACAGTAAAGA ACTGATGAAC 1920 CATAAAAAGA AAAGGTTAGA CAGACAGCAG ATTAGTGGTT GCCAGGTGCT GGGGGTGGGG 1980 AGAATGCTGA GTGCTTCACA GGAATGAGGA CTCCTTTGCG GGTAATGAAA ATGTTTTGGA 2040 ACTAGACAGA AGTGGTGGTT GTGCCGAATT GCAAATGTAC TAAATGCCAC CGAATTTTTC 2100 ACTTTACAAC AATTTCTTTT ATGTTACATG CATTTCCCCT TAGTTACACA CACACACACA 2160 CACACACACA CACTCACACA AACTAAACTA AACTAAACTA ATTATATTAA ATGAGAGAAG 2220 CCAGGTACAA GAGTACAATC TATAAGCCTA GGTATATGAG GTTTGAGAAC AGGCTAGAGT 2280 ACACTATGGT GATAGAAATT AGAACAGTGG GACGGGTGTA GTGGCTCACA CCTGTAATCC 2340 CAGCACTTTG GGAGGCCAAG GCGGGTGGAT AACCTGAGGT CAAGAGTTTG ACACTAGCCT 2400 GGCCAACACA GTGAAACAGT GTTCTCTACT AAAAATAACA AAAATTAGCT GGGCGTGGTG 2460 GTGTGCGCCT ATAGTCCCAG CTACTCAGGG GGCTGAGGCA GGAGAATCAC TTGAACCCGG 2520 GAGACAGAGG TTGCAGTGAC CCGAGATCAC ATCACTGTAC 2560
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