Tag | Content |
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EnhancerAtlas ID | HS052-27765 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr3:183024250-183025720 |
| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_27019 | chr3:183024136-183025985 | Esophagus | SE_51479 | chr3:183023859-183025861 | Skeletal_Muscle |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr3 | 183024720 | 183025033 | chr3 | 183024502 | 183025396 |
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| Number: 1 | ID | Chromosome | Start | End |
GH03I183305 | chr3 | 183022880 | 183027942 |
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Enhancer Sequence | CTTTATTGAA ATAAGTTTAT TTCCCCCCGA GGACTCTGCT GGTATAACAG ATGAGAGATG 60 AGAGTGCCTA CTAGGGAAGA AAGTGGCGAG AAAGCGAGTG ATGCTACTCT ATCCGGGAAT 120 CTAGAACAAA CCCACAGAGG ATCCACAGGG ATGGAGTGTG TGTATGGGGA GGTGGGCCAG 180 ATGAAACAAG AAAGGCAGAA AGCTAATGGT TGTTGAAATT GAATGATGGA CACTTGGAGT 240 TCATTGTGCC AGTCTATCTG CTTCTCTGTG TGTTTGAAAA TTTCACACAT GTACACAAAG 300 CCATGACCCT CCAACAAGAT GACATCCTTA GATGTTAATG GCCTGGGTTC CATGCCTTCT 360 TAGACACAGC ACCCTTATGG GGAGAGGTCA AGGCTGAAAT CAGGTGGTTC CTCCACCCTG 420 TCCTGGTCTG TTCCCTGCTG GCCCCTCAGC AAGGGTCTCA GTACGGCCCA CAGTCAAAAC 480 CCTGCAGCAA GTTCTGCTTT TATAGAAGAC CTTCTGTAAG TGGTTGAAAC TACTGTTTTT 540 CAGAATCAGG AAGGAGCATT CAAAAGACTG CTAAACCCTC AAACGAGAAC AAGATAAAGA 600 ACAGGCTGAA TCAGCATGCG ACAGGAGCCT GGTTAGTGAG TTGACTGAGG TTACTTGTGA 660 GAATGATGTC ACTGTGTGGA ATAAGGAAGC TGGCAACACC CCAGAGCCAG CGTGTGGCTG 720 TGCTGGGAGG GAGCTGGCCC CTTAGTGCCG AGTAAAGGAC AAACTCCAGG CAGATATTTG 780 TCAGATTGTG GCCAGACACA GTCTTGTTCC TTTAACACTT TAAAGGACAA ATGGAAAGAT 840 TAGCCAAGCC CTAATCATCT GAAGAAGCCA TGTGTCTGAG AAGTCTGAGG GAAGATATAT 900 TGAAAACGAT CTCAGTTACG ATGAGACAGC TTTGTTTGAT TTACGCAAAG GCAGAGACAC 960 AGGTGTACTA CATCCTTCAG GAAGCAAGTT TAGAAATAAG ATCTGCAAGT CATAGGATGT 1020 GACAGGTCTG CAAATCCTGC AAGTCACAGG TCATCCACAG TGGGCTAGTC TAGCTGCTTC 1080 AAGAATGTTG CCCACGAAAG GTGGGTCATG GGTTCACAGA GCATTCCTGT GTTCCATAAC 1140 CACAGGTTTC ATCCCTAACT CTGGTCAGCA ACTTTTGAAG TATATACCAA GGACCACAAG 1200 TTCAAGGAAG TGGGCAGAAG AAAGAATGTG ATGCAGTCAT GCAGATCCAT CGCCACTATT 1260 CAAGACACAG CCCAGAGCGC CTTCCAAGGG CTTTCTGTTC CACTGAGAAT AAAATTCAAA 1320 TCCTCACAAA AGATCTCAGG GTGCAACAGG ACTACCTGGC CTCTGCTCAT CTCTGTTCAC 1380 TCATTTCCTC CTGGCCCACC TGCTCTAGCA ATGTTCCTTG AACTCACCAA GCTCATTTCC 1440 ACTTTAGGAC CTTTGCACCT GCAGCTCGCT 1470
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