Tag | Content |
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EnhancerAtlas ID | HS048-27314 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr4:6993990-6995500 |
| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27343 | chr4:6992023-6995626 | Esophagus | SE_27664 | chr4:6993890-6995431 | Fetal_Intestine | SE_28549 | chr4:6993721-6995625 | Fetal_Intestine_Large | SE_36318 | chr4:6992335-6995784 | HMEC |
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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 |
GH04I006990 | chr4 | 6992502 | 6995582 |
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Enhancer Sequence | GCAGAGGCCA CACCTAAGCC GTGTAGGACT CGGGCTTTCC CCTCTAAAAC TGCACACCTG 60 TGGGTTTGAG TGTATTCACA GATGATATTG GGCCGGCTCA GGGCGGCAGG CCCAGCCTTG 120 CTGGCTGTAT GCTTCAGGCA AGTCACTTCA CTTTGAGCCT CAGTTACCCT GTCTTTAAAA 180 TGGGTAACAC TTGCCAAGCA GATTGCTGTG AAGACAAAGT GAGTCCACAT GCACAGAGCA 240 CACAAAAGCC GATGGAAATG GGCATCCACA TCCTGCCATG GCTGATTTTG GGCCCAGCAT 300 TCTGGCCTTG GCATACAGTT CACCAGACCA GGCTCAGCAG ATAAGTAGCA CCTCATGGGG 360 TATGTGTTAC TAATTCTTGT TAAAATGCAG CATGCCTCAG AATCTTTCTC AACACACAGC 420 TTTTGTTTGA TTTCCTATGA AATTGGAGAC TTTGACATTC AGGTGCTAGA CTTGAAGCTT 480 CATGAGGGCT AGTGCCGTCT TAGGTCACGG CTGTGTACCC CATACAGTGT AGATGTTCAG 540 ATGCTTGAAT CCAGCAAGGA ATGAGTCCGT GTTTTCAGTT TTTGGTAAGT GGAAGTAATT 600 TTAGAATTGT AATGAAACCA TGTTAAGCCA CAGTAAACAG TGTTAAGACA TGTGACCATA 660 TACATCCAGG TGTACAGAAA CTGCCCCACC CAACTGCTTC TTGGTGCACG TCCTTCTCAT 720 AGCCTGTGTA TTTTGAGGAA ATAATCTATT TCTTTATACT TTTTAGAGGC CTTTCTGGCT 780 AAGAGAATAA TTGCTTGCCG CATAATTTCA CCAGTAACAC GCCTCTTGAC AGCTAGTTTC 840 CCTGAAATTC ATTTAGCAAT TTCTCACCAC CTCATGACAA ACATGAAATC TTAGGTTAAC 900 ACTACCTTCT TTGTCCTATC TTCTCAATGA GATTATCTTC CCTTCAGGGG CATTCCTGAG 960 AGCCTTGTCT GTAATATTTC CTTAATTATC TATAATCATC TTAAATGATT GTGTTTTTTG 1020 ATTTTGCACA GAGCGAAGTA CCTACACATT ATTTCAGAAG CACCAACCTG TTTGGCTCTC 1080 CTGAGTTCTT CCAGCTGGGC GTTTGGAATG TGGGTCACCG GGTGTGAATG AGCTCTTGTG 1140 GTTGCAGTGC ACGGGTGAAT CGGTGACCCA GTGATGTGGA GGCTGCTCTT AGATTTCCAG 1200 GGCATGGCAA AACTATTTAC ATAACAATTT GCAGTGGCAG CTTCCCAGTG GCCGTGATAA 1260 TAATCAGTTA AAATTTACAG TGTCCAGAAG AGAGAAAACA TGCCTGTTAC CCAGGAGACA 1320 GTAGACCTGA GGCAGCGTTT GAGGGCCCTC CTCAAAGGGG CTGCTTTGAT AATGAGATCC 1380 TTTGTTATTT CCCCACCAAC GAGGGAAGCG TGCAGTCATA TCATAAAGCA ATGGTCTCAG 1440 CTTTGGAACT CTAAGACCCC TTTAGGCTGG GCACAGTGGC TCACGCCTGT AATGTCAGCA 1500 CTTTGGGAGG 1510
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