Tag | Content |
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EnhancerAtlas ID | HS023-17071 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr22:29217400-29220050 |
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 | CCTATGCTGG AGTGCAGTGG TGTGATCATG GCTCACTGCA GCCTCCACCT CTCAGGCTCA 60 TATGATCCTC CTGCCTCAGC CTCCCAAGTA GCTGGGACAA CAGACATGTA CCACCATGCC 120 CAGCTAATAG GGACTGTATC TTATGTATGA ACCTTTGTAA CTCTCAAGCC ACTTGATAGC 180 CCTCAGTAAC TATTATTGGC CAAATTTGTC CTTTTTGGCA GAGCACCTGG CAGGGACTCA 240 GTACATCCCT AATCAGTTGC TCATCTGAGG CACAGAAAGG TTAAAAGTGA TGCAGCCAGG 300 ACCTGCTGGC AAATCCCCAT GGCTCCAGCA CCAGGCCTGT CTGGCTCCTG AACCTCTGAC 360 CTACTGCTGC TCATCCATAT CTATCTCCTG AGACCTCGAG ACATGAATCC ACCTTGGGTA 420 ACCTGTAAAG ACTTATTTGC CTAAAACCTG CCCAGGAGTC TTAATGTCCC CATCCCGTTT 480 TAATAGATGA ACACTTTGCT TTTGGAAACT TTCTGTTCCT TGGATATTGA TGGTCATATT 540 GCTTCTGGAA TCATTACAGT GTGCCTTCAG CCAAAAGCAG AACTGGAAAC ATCCTAAGTG 600 GGCCGGTAAC GAGGCTAGCT CTGTCGACTA GTTCAAGACC CCTGAGCGCT TTGGGCCTGA 660 GGTTCCTCAG CTTCCAAGTG AAAGGCTTCG ACTTGGCATT CTAAGAGACA ATCTCTGTGA 720 CCATCAGTTT CCTCATCTGT AAAACTGGCA TCATGATAAC TTTGAAGGTA ATTGTGAAGA 780 TTAAAGGGAG TCATGCATGT AAACCACCTT GCATAGTCCC TTGTGGGAGT TCTTGGTTTT 840 TTGTTTTTTT GGGGTTTTTT GGTTTGTTTG TTTGTTTTGA AACAGAGTCT TGCTCTGTCG 900 CCCAGACTGG AGTGCAGTGG TGCAATCTCG GCTCACTGCA GCCTCCACCT CCCTGATTCA 960 AATGATTCTT GCACCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCGCCTG CCACCATGCC 1020 CAGCTAATTT TTGTATTTTT AGTAGAGACA GAGTTTCGCC CTGTTGGCCA GGCTGGTCTC 1080 AAACTCCTGG CCTCAAGTGA TCCACCTGCC TCGGCCTCAC AAAGTGCTAG GATTACAGGT 1140 GTAAGTCACC TTGCCCGCCC GGGAGTTCAT TTATTAGCTT GTTTTTCCTT CTCCTTCTCC 1200 TCTTAAGTCT AAACTGCAGT GATTTTATGA TTCCACTTTT CGAGTCAGTG CCCCAGATGG 1260 TTTGCTCATT CATTCATTCA CCCCAAAAAA TGTTTATTGT TCACCTACTA TGTGGCAAGC 1320 ATCACACTAG GTACTGGGTG CTAAGCATAT GGTGGTGGGC AAGAACCTCT CTAGAAAACA 1380 TCAGAAATTG TCCAGCAATC CCCAGCAATG CAAAGAAAGA CACAGCAAAA AAATGCATGA 1440 TCAAATGCAT CCAGAAGTCT GAAATTATAA CTTTTATAAT TGTTTCAAGT GAATTCTGAG 1500 TAGATGCTAC TTAGCAGGTG GCCACAGTTC TCCCCAGTAG CTGCTGTTCC ACTTAAGACA 1560 CCTGCTGCTG TTTCCAGGAT GCTAACATTT ACTTTGGTCT TTATGTCAAT GTCATTTGCA 1620 GAGAGAGCCA GCTGTGTGGC TTTTTCTCTT TCAACATTGC CACTGAATTG TGCTTTGTTG 1680 ACAGAAATTA AACACTGCTC ACGTAGATAG CATCAGGGCA GCCTTCAAGA CTGGTTTGAA 1740 CAGGAACCTT CTGCCCAAGA TGAAGAGTAG ACTCTATCTT GGGGTTAGGA ATGTTTTCCT 1800 TCTTTGTGGC TTGATCATCT GGCCAAATTT TACTTTACCT AGTGCTGCTT TTGTTCCCCT 1860 GGCTTTCCTT CCTTGGAGCC CTTTTAAAAT AATCCTTCTC TGCTTGTGGG ATTTTACCAG 1920 ACAGTAAAGA ACTGATGAAC CATAAAAAGA AAAGGTTAGA CAGACAGCAG ATTAGTGGTT 1980 GCCAGGTGCT GGGGGTGGGG AGAATGCTGA GTGCTTCACA GGAATGAGGA CTCCTTTGCG 2040 GGTAATGAAA ATGTTTTGGA ACTAGACAGA AGTGGTGGTT GTGCCGAATT GCAAATGTAC 2100 TAAATGCCAC CGAATTTTTC ACTTTACAAC AATTTCTTTT ATGTTACATG CATTTCCCCT 2160 TAGTTACACA CACACACACA CACACACACA CACTCACACA AACTAAACTA AACTAAACTA 2220 ATTATATTAA ATGAGAGAAG CCAGGTACAA GAGTACAATC TATAAGCCTA GGTATATGAG 2280 GTTTGAGAAC AGGCTAGAGT ACACTATGGT GATAGAAATT AGAACAGTGG GACGGGTGTA 2340 GTGGCTCACA CCTGTAATCC CAGCACTTTG GGAGGCCAAG GCGGGTGGAT AACCTGAGGT 2400 CAAGAGTTTG ACACTAGCCT GGCCAACACA GTGAAACAGT GTTCTCTACT AAAAATAACA 2460 AAAATTAGCT GGGCGTGGTG GTGTGCGCCT ATAGTCCCAG CTACTCAGGG GGCTGAGGCA 2520 GGAGAATCAC TTGAACCCGG GAGACAGAGG TTGCAGTGAC CCGAGATCAC ATCACTGTAC 2580 TCCAGCCTGC GTAACAGAGT GAGACTCCAT CTCAAAATAA ATAAATAAAT AAATAAATAA 2640 ATAAAGGCTA 2650
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