Tag | Content |
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EnhancerAtlas ID | HS048-20922 | Organism | Homo sapiens | Tissue/cell | Fetal_small_intestine | Coordinate | chr2:102470720-102472430 | | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_45627 | chr2:102470233-102472087 | Osteoblasts |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH02I101854 | chr2 | 102470725 | 102472297 |
| Enhancer Sequence | ACAAACAAAA AGTGAGATGA GTAATAACAC CTTGATAAAT AAAGATGGCA TAGCCATTAA 60 AGTTGTAGTT TTTAGATACT AGAGCAGGAG CATCATTCAT TTTATGACCC CATCTCCACC 120 CATGGGAAGC TGATGAGTTT TGTGTATTGA ATTCGAAGAG CAGAGAATGG GGGAAAAGGA 180 GATTCCCCCA TTGAAAACCT AGATAATGAG AGAGGCGGAA CCAAAAGCAG ACTCAGAACT 240 TCACTGAGAA TAATGGGGGT GTAGTAGTCA GGTGAGAGAG ACTGGACTAC CAAATCATCG 300 TTGCTATCCA GTTATTCCAG ATGAAAGATA CTACTTTACA TTTCTTAGGG CATCATTTTT 360 AAGTGTTGGC TTTCAGATTA AATACTAGTT GAGAGTGGTG GGAAGACCCA GAAGGAATAC 420 TTAAACTATA ATAAATATGT ACTTTGTGTA TCCATTATAA ATATGTCTAA CATCCCTGAT 480 AGCTTTACCC TAAGCTTTCT TGTTTAATGG TTAATTTTAG TGTCACAAAT AAAGTTTGTG 540 TTAATATTAT TGGCTCTCTG TGTCTGGGAA ATTTGATGGC TGTGCATCCC CTAGAGTTGC 600 TGCTACCCAG TAGCCACTAG CCACATTTGG CCATTTAAAT TAAAATTAAC TTCAGTGCAA 660 CAAAATTAAA AACTCAGTTT TTCATTCATG CTAGCTATAT TTCAGGTGCT CATTAGCAAC 720 ACGTGACTAG TGACTACGGA GCAGTGCAGA GACAGAACAT TTTTATTATC CCAGAGAGTC 780 CAGAGTCTAG CTTGTGCTTT ACTGGCAGAC AGCCTTGAGC TAGAAGAGTG AGTTGTCATC 840 ACGTGCCTGG CATGTCATCT TGCTCTGTTC TGTAGGGTTA CATAGAACAG TCTGGATTTA 900 GAAAGGCTGA GTGAGTCTGG TGATTCAGTA GCACCTTTTA CACCTGTTGA TGGGATGCAG 960 GGTAGAGGGT GGTTAAGAGT ATGTATGGGC CGTAGAGGCA GAGCAGCTCT TCCAGCTGGG 1020 GGCTTGCTGG CTGTGTGACT TTGGGCAAGT CACTTACCTT TTCTGAACCT GCTTTCGCAT 1080 CTGTAAAGCA GGGATGAAAT AATGACTTCC TTGGGTTGTT AGGAGAATTA TATTAGGTAA 1140 AGTAAGTGGA ATAGAAATAT CAAATACTTA GCATAGTGCC AGGCACATAG TAGTAAGCAT 1200 TTGCTCAGTA GCAGTTTCTG AAATACTTAT ATTAATAATA ATGGTCCTGG TTATTCTTGT 1260 TGACGTCAGT TCCTCTTTTC CTGATGTGTG CTTCTTTTTT TCCTTTTTTA AATTCTTTGT 1320 CTGTCTTTGC TGTATTTCTA TTTCCCTTTA TTTCTTTCTC TTAATGTATT TTTCTTCTGA 1380 CTTAAGGGTC CTGCATAACC CTGTTAATGA TATCCACGAA TAAAGAATTT TCTGTCCCCT 1440 AATTGCTGTG GTGCAGTGAG CAGTGGGGAA TAATTGTTAT CAAAATGAAA CTAAACCCTA 1500 TAAGGATTCA CAGAGTCACA ATACTTTTGA CCAGCATTCA TGAAGAAGCC CTTACTTATG 1560 GGTCCGAGGG GCAGTGTGGA AATAATTGGC CAGTAGATAT GGGGCCCATG AACCTCACCT 1620 CATTAGTGTC CACCTGGCAC TGACTGATCA GCACACTATA ACATCATGAG AAAGATGGCG 1680 GGAAGATCCC TGGTAATTAT ACATTTTTAC 1710
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