| Tag | Content |
|---|
EnhancerAtlas ID | HS060-13368 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:70449990-70451490 |
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_10808 | chr16:70450197-70451719 | CD19_Primary | | SE_27776 | chr16:70448923-70457488 | Fetal_Intestine | | SE_28634 | chr16:70448899-70457647 | Fetal_Intestine_Large | | SE_32687 | chr16:70449734-70453680 | GM12878 | | SE_35582 | chr16:70450535-70453802 | HepG2 | | SE_39873 | chr16:70450007-70451076 | K562 | | SE_53222 | chr16:70450475-70455599 | Small_Intestine | | SE_59329 | chr16:70441356-70474175 | Ly3 |
|
| | 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 |
| GH16I070414 | chr16 | 70448014 | 70458303 |
|
Enhancer Sequence | TAACAATCAA AAGGAAGCAA TCCTACCTCC ACTCTCTTCC TCCCGGATGA TCGCAGTGTT 60
GGTTACTGCT GACCACCACT GTGATTTCCA GTTTTACCTA TTTCTTTCAG CTGCTAATGT 120
ATTTCAAAAG CATGAGATGG GGTGCCCTTA TTCATGCAGC GAGGTCAAGA TCTTAACATA 180
AATAGCATTC AGAGATGCCC AAACCAGGCC TCCCCAGCCT CATCTCTTAT CAGACCCTAT 240
TCTCTAAGGT TTACAAACTA ATTTGGATCC CAAGCCAGAA CTGGCCCACA TTTATTAAGA 300
TTCTACACTG AAACTAAAAA GACATGTATG TGTCTCTCAC TTAAAAGAAC CCTAAGAACT 360
CTCAGGGTAC AGAGACAATG CTATTTAATT CCTCATCTCT GTACCACTGT AGCGCCTAGC 420
ACTGTCCTGC ATATAGGAGG CATCAATAAA TGTTTGCCCA ACTGAGTATC ATCTCTCTAC 480
ATAAGCCCAG GGCTATAAAA ATCAAAAGAA ATGATGGTTA TAAAAAATGC TTTGAAACCA 540
TTATTATGAA TTATATAAGT ATGCATATGA AAGTGATAAT TATATTCTGC CCCCACTTTT 600
CCATCTCTGA CATTCTAGAA GTGAGAGCTT TCTCTAACTT CTCTTGGACC ACCCAGAAAC 660
ATGAGACCTC AGGTACAAAC CAAATTGAGC AAATCTGAGC CTGTGGGAAA GGGGTGTGCG 720
TGTAAAGCTG AAGCAGGTGC CTGGACGACG GCAGGGACAG TGGGAGTGTG CTACTCTTAA 780
GGGCCCAGCA ACAAACACCT GGCACGGCTG CTGACCTGGA ACTCCTGCAG CTCACTCCCC 840
TAAGCACCGC AAGCTGCAGT CCTCCCAGCT GGGGCTTTCC AGATCACTCA CCCGTTCACC 900
TCGGCTCAAA GCATCTCCAG ATGAACAAAG TGCGTAGAAA AACTTGGATT CACATTGTGG 960
GTTTGCCACT TGTCAGCTAT TGACCATGTA ACTTCTCTCA TGGTCCTGAT CTGTGCAATG 1020
GGAATAGCAC CCATCTCGAA GGGGTTCCAT GAGGATTATA TAAAGGCACA CATAAAGCTC 1080
TACCTCCATG GCTATGGTCA TGGGTTGGGC AGATTGAGGG TCACAGCTCT GCAGGAGCCC 1140
CATGGCATCA CAAGGAAGGC ACAAACCCCT CCCACACAGC ACTGACTCTG GCTCCACAGC 1200
GCCCCAGCCC CACCCCACCT TCCCAGCCCC CACTTCCCAC AGGAACTCTC CTCCCTGGGG 1260
CCCCACTCCC AGCAGGCACC GGCCTCCAGG AAGGTTGCGG TTTCAGGGCC AGCCCTACCT 1320
TGGTTGATCC TTGCCCCTAG ACCCAGCAGA GGACGGTGCG CGTCCATCCT ATGGGACACG 1380
GCCGTAACCC CTTCCCCAGC CCCCACTTTA GCACACCCTG CAGAGCAGAG GCCTGACCTG 1440
AGCTGGCTCT AAACAGCTCC CTGAGGCTGG AGGCCAGACA GCCACAAGCC AGGAGCAAGA 1500
|
