| Tag | Content |
|---|
EnhancerAtlas ID | HS037-22119 | Organism | Homo sapiens | Tissue/cell | ESC | Coordinate | chr2:239195800-239196980 | | | Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
| SE_23101 | chr2:239193088-239200603 | Colon_Crypt_1 | | SE_23739 | chr2:239193087-239200559 | Colon_Crypt_2 | | SE_24713 | chr2:239193091-239200611 | Colon_Crypt_3 | | SE_27053 | chr2:239193008-239200522 | Esophagus | | SE_28235 | chr2:239192879-239199789 | Fetal_Intestine | | SE_29205 | chr2:239192959-239199819 | Fetal_Intestine_Large | | SE_31544 | chr2:239193018-239200823 | Gastric | | SE_36465 | chr2:239193425-239200323 | HMEC | | SE_37617 | chr2:239193371-239198450 | HSMMtube | | SE_47604 | chr2:239193144-239198901 | Pancreas | | SE_50608 | chr2:239193103-239200505 | Sigmoid_Colon | | SE_52761 | chr2:239193002-239200250 | Small_Intestine | | SE_64528 | chr2:239193704-239200417 | NHEK | | SE_65405 | chr2:239193384-239200431 | Pancreatic_islets |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGGCTGCGT TAGTTCTGTA CCAATGAATC ATACCAAGGC GACAGTGACA GATAACTGCA 60
AACACCCACG GTGCCATCCC CGCGCTGGCA CACCACACAG CTTCCACTCA AAAAAAACGG 120
AGTCCCTTTC TTCATTATAG TCATATAGCA CACAAAAATC AATTCACCTT GTATTTTAAA 180
ACTCAATTTC CAAATAAAGC CTTCAGGTAG AGTCCTGTTT TCTTCTCAGG CACACCCAGC 240
CTGGGACCAG AAGCCCCAGG TGGGGGTAGA GGGTGGGCCA AGAAGTCTAG CAGTCCTGCT 300
GTGCCATATA CAGGTGAGAG GCGTCCATGT GGGGCTTTAG CCACCGTGTG GGGTTCTTAA 360
CACATTTCCC GGACTTAAGG CCCTTCCTCC CAAATTCCAG CCCACCCAGG ATTCAGCACG 420
CAAGTGGAGG CCATCACTGA ACCTCTGAAG CTCATCCTGC CCCAGGACGA TGGGAAGATC 480
CTGCAGACAG CCTGGGCCTG GGCCTCAGTT TGCTCATCTG TCAGGCTGAG GGGTTACTCT 540
GGGTGATTTT CAGGGTGCCT TCTGGCTCTG TTGTTCTGTA TGAATCAGCT TTCCAAACGG 600
GTTCCTTCTG TGTAGGTTAC AGAAACCCTG GCAACCAACT CGTCATCCCT TACCCTGGCC 660
TTCCTGAAGG GGGAAGCAGG CCACCTCCCA CCCCCTGGTC TATGTCTGGG ACTTGGCAGC 720
CAAAGTACAT CCCAGAAGGT AGGCGCGACT GCTGCACCAA AGAGTGGACA CCCCCATTCC 780
CTTCTATCCA GTCCGGGGAA AGGGAATTAA TACAGGGTGG TCCAGGGGAG GCAAAGGGGC 840
GAACATTAGA GGGTCTCCCC GCCCTCAGGT TCCCAGGCCT GGCTTGGCAC CGGGACTTCC 900
TTGTCCCTCT GATCACCCAT TCCAGGAGAC CCGTGGGTGT CCAGGAAAAG CTCCTAGATC 960
AGCGCCCCTC CATGGCCCTT CCCCAGCCCA GGACTTAGCC CTGTGGCCTC AGAAGAGGCA 1020
GTCAGCTCCC CGAGGGTCCT CCAGATCCCA GGGCCGGCTG CGCTGACCCT TGGTTTCCTT 1080
GGCCTTCCCC ATGCGAGGGG AGGGAGGGTT CCCAAAAGAG AATCGCCCAC GGAACCGCAG 1140
CCCGCGCGCA GTCACTCGGT AGCTCGGTGC CCTACACACG 1180
|
| |
|
|
|
