| Tag | Content |
|---|
EnhancerAtlas ID | HS095-11573 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr16:68524610-68525950 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr16:68525300-68525321 | GGGGCAGGAGGGGAGGGGAGA | + | 7.29 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_52879 | chr16:68523558-68528354 | Small_Intestine |
|
| | 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 |
| GH16I068489 | chr16 | 68523808 | 68527942 |
|
Enhancer Sequence | AAGCAATCCC CCTGCCTTGC ACTCCCAAAG GGCTGGGATT ATAGGTGTGA GCCACCATCT 60
ATGCCAGCCA AGGTTTGTGT TTTAGAAAGA TCCCTGGCAG GCAATATGGA GAGTGATTTA 120
GAGCCCAGGG AGCTTATTAG GAGGAGGTGA GGGAGGGTCT ACCTGGGCAG TGTGTCAGGA 180
AGACAGGGAA GGACAGATGT GGGGTGAGGG CAGAGGACAG TCAGCACATC GGTGCTGCCA 240
ACCCTTTCCT CTCATGGCTT CAGCAATGCT GCTCTCACCG GTTCCCACCA CACACTGTGT 300
GCGTAAATAG ATGGAGGGGT GGTGGGAGGG ATGGGGGATG GGTGTTTGGG CTCAGGGGCG 360
AATCTTGGAC CGAGCACTGT GAGGTGACGG TGGGGCCAAG GCTTGCATCT CCCCACCCAC 420
CTGTCCACTG CCATTGTGGA GCAGCCAGTG TGGAACAGCC AGGTGCGGGT GGGGACTGCA 480
GGTGTCCTCC CCAGTCCAGC AGGAAACCAC TGACTCATGT CTGACAGCTC TCAGCCTGGA 540
TGGGCTCCCG GAGGCTGTTA GTCACCTGTG AAACAAGGGC ACGTGATCCC TTCTTGCCCT 600
GAATTCCTCA GGCTGTGGAC TCCCTGGGAC CACAAGTTTG AACTTCTAGG AAAGAAGGGA 660
CTCAGGTTTT TTTGGAGACC CCCATCCTCA GGGGCAGGAG GGGAGGGGAG AGGAAACCCG 720
AGCCTGGTGA GGAGGTTAAA AGTTTGAACT TGATCCCTGC CAAGGAGGAG TTGGGTCTCA 780
GCTGTGATCA CTGAGCCTTT GCATCCTGTA ACCTTTTTCT GGTTACGCAT GGCAAGTACA 840
GCACTGGCCA GGCACGTTTC TGTCGTTTAC ACTGATCCAC AGAAGCCTCT GTCCACAGAC 900
GACCTCAAAA TGGCATTCAC CGTAAGCAGA ATTCACCTTC AAAACGCTAC GTGAGTCCAG 960
GGGGGCAGCG AAGAAGAGGC CGAAGGAGCA GTGGGGCAGG GGTCGCGGGT CTCTGTGGTG 1020
TGGAGGGGGC AGCGCCGGGA ATGTGCGGGG AAGCCTGGAG GCCTGGGTCC CAAGCCCCTG 1080
TGCCAATTGC TGGGGGCCCA TGAGACTCAC TCCACCTTGC TGAGCTGATT CTGGACCCTG 1140
ATCACAAGGG ACTGCAAATC CGTGTTCTCG TGCCTTCAAT CTGGGCCTGC CAGGGTTGAG 1200
ACACGGCACA GACCCTCTGA GTTGGCTTTG GGAAGATAGA TGGAAGCCAT TCCCTCTTGC 1260
TTCTCCGGTG CAGGCTGCAA CTCGTCAGCC AGTTGATACC AAGTGTTTAC AGTGCATGAA 1320
TCTCGACCCG AGATCTACAA 1340
|
