Tag | Content |
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EnhancerAtlas ID | HS095-07147 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr12:53253330-53254490 |
| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23067 | chr12:53253409-53254482 | Colon_Crypt_1 | SE_23945 | chr12:53253372-53254058 | Colon_Crypt_2 | SE_23945 | chr12:53254104-53254500 | Colon_Crypt_2 | SE_26564 | chr12:53252201-53257552 | Esophagus | SE_27647 | chr12:53253176-53254798 | Fetal_Intestine | SE_28539 | chr12:53253238-53254737 | Fetal_Intestine_Large | SE_56286 | chr12:53253248-53254286 | u87 | SE_64566 | chr12:53253134-53255265 | NHEK |
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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 |
GH12I052859 | chr12 | 53253290 | 53255117 |
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Enhancer Sequence | CCTTGCTCTA CAGACACAGA AATAAAGCAA TTGTCCAAGA TCTCAAAGAT GGAAAGAGGC 60 CAAGTTAGGA TGAAAACCCA GATCTTCTAA ACATACACCG CCCCAATAGT CTTCCCAGGA 120 ACACTGTACA GCCTTCATGT AGTATGTATA TGTACATGTT TCCTGTATAA CAAAGAGACC 180 AGAAGCTTCC CTGGTGCTGG GGGCTATGGG GAGAGCCCAA GGGAGAGGAC ACCCGCTCCC 240 ACTCTGCTGC AACACACAGC ACTCTGCTCA GGGATGGGGC AGTGGCGTGT TATTGTTACA 300 CAAGGGGCTC TCTGTCAGGG AGGGAAGATA AGTCTGTTCT GTAGTGTTTG CCATTTTCCG 360 TGGTGCAAAT ATTCCATGGC TGATTTCAAG CTGCCACCAT GATGTCACTG AATGCAGAGC 420 TGGGAAGAGA TGCACACAAT CAGGTCTCCT GAGTTTGCTC AAGCAGGCCC AGCACACCAT 480 GGGCCAGGGG TGAAGAAAGG GAGACTGTCC CAGGCTGGGA GTCAGGAACA CACATCCAGG 540 AACAAACTGC TGGTGCCTGA GAGAGGAAGG GGATTGGACA AAGCTTCCAA CTCTGGGGGA 600 CCCTGAGAGG GGAAGAGGGA AGTGTTCAGA CAAGAACTTG AGTTGAGAGT CCAGACACAC 660 CCATCCAGGG CTTAGTACCC AGCCACTGCA ACCCTGACCC AATCAGGTTC AGCCAGTTGG 720 GTGCCCTGCT GCTAGCAACA GCTCCTGATT TGGCAAATAT TATGAGGCCT GTTACTAAGG 780 ACAGCCTCCC AATACCCCAG AGGGTGAAGA GCAACTTCCA GGGGAAAGTT GCCAAGATTC 840 TTACACCCTG AGGATGTTCA GTCGAAGCTG CAGCAGGAAC TCCCGGACTG GGAGACAGGG 900 TGGGGGATTA CATGGACCAG CTCCCTCCCA CTCAACCATC TCGCCAGCAT CTCTCCCATG 960 GCCATCTGAG TGCTGTGCCC TGGGTGTTGG AAGTAAGGTT CTGCCCGTCT TCAAGGAACT 1020 TCCATCTGAG AGGAGATCTG TATTTTCAAA ACTGCAAGCT ACAACCCACT AGTGGATTGT 1080 GAAATCAATT GCATGAGTCT TTACCAGCAC ATGAGTGTGC ATCACAGGTA GTAAGGGTAA 1140 TATTGCACCA TGAAATTTTG 1160
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