| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02261 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:204282810-204283920 |
| | Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
| SE_23313 | chr1:204283017-204284108 | Colon_Crypt_1 | | SE_24138 | chr1:204282905-204283426 | Colon_Crypt_2 | | SE_28816 | chr1:204282582-204285217 | Fetal_Intestine_Large | | SE_31690 | chr1:204282936-204283957 | Gastric | | SE_33663 | chr1:204282160-204285331 | H2171 | | SE_37243 | chr1:204283266-204291796 | HSMMtube | | SE_50227 | chr1:204282848-204284237 | Sigmoid_Colon | | SE_52903 | chr1:204283402-204284220 | Small_Intestine | | SE_65374 | chr1:204282543-204284287 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 4 | Chromosome | Start | End |
| chr1 | 204283200 | 204283400 | | chr1 | 204283400 | 204283800 | | chr1 | 204282931 | 204283054 | | chr1 | 204283310 | 204283744 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204313 | chr1 | 204282903 | 204286933 |
|
Enhancer Sequence | AGATTTTCAC CTGACATTCT GCAGCTAACC ACCTTTCTAT CTGTCATCTC CCTGGGAGAC 60
ATGGTCATTA GCAGAGAGCA CCATGTAGGT GTCTAATTAA GCAAGCAGCA GCAAATGCAG 120
AAACCTGTTC AAGCCACCCC ACAGAGCATC TCCCCGGGGA TCCTCTTACA GGCAGCTCCC 180
TCCCCCGAGC TTCCTGGAAA GGTCTCTATT GTTTGCCTAG AACACAGAAA AGTGTCCGAT 240
TCTGCCCTCC TACTTATCTG CTGGCACAGA CTTCCTGGCC TCTGCACAAC CCCAGGGGGT 300
ACTATTCCCA TATAGCACAA TGTGAACGGT GCCCTCAGAA TTGTGGGACA CAGCAGCACT 360
GGTGGGTGGG AAAGTGAGGG TCCCCAGATG GGGAGGGACA GGATCTTCTG AGGGATGTCC 420
TCTTACCTGT CTTCCTTAGG GGTCCCAGAG CCATATCCTG CCATCCTAGC ATCTTGAGAT 480
CAGGGCACAG GAAGCAAGGT GCCCTCAAAC AGATTGATAA TAAGATGGCA GAGACAGAGG 540
TGGACAGCAT GAGTGGCTCA GCCACTCCCT CAACCTGTGT CTCAGAGTCC TGTTGTCTGA 600
ACTGTAGCTC ACCTGTTCCT GTTTCACCCT TCAAATGGAA TGTTCCACTT CCCCTGTGAG 660
CCCGGGGAGA GAAATAAATT CCCTGTTCTA GAAAAGCTTT CTTCTTTAGA GACTGAAGTC 720
TCTGGAATTT CATCTAATAC TCCTGCAGAC GACAATGGAG TGACTGGGCC AACAGTAAGT 780
GCAGAGAAGG ATCCTGGAAC GACAAGACTG ATCCTAACTG GCCACCACTC CCCCTGGCCT 840
GGGGATGGTC TAACCAAGGA GACTGGAGGG GAATAGACAG ACACCTGCTG CCTCTGTAGC 900
TCCTGGCGGA CCTCACTCTC AGGTGTCAGA TGAGTATCCC AACCAAGCTG GGGCGAGAAA 960
TAGCAGAATC CTCCTTAACT TCTTCTCCTG TGCCCTTCCC TGAGTCAAGC TTGTCTTTCT 1020
TCTAGGCCCT TATCTCCCTG CCTCAGAGAC CTTTATCCAC TTCATCTCTT ACCTCCACAA 1080
TGGCGCAGGG GCGGTAGAGA TGCTGGTATG 1110
|
