| Tag | Content |
|---|
EnhancerAtlas ID | HS118-08386 |
Organism | Homo sapiens |
Tissue/cell | Liver |
Coordinate | chr17:73990570-73991990 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:73991566-73991581 | ACAGGTGAGAGGTCA | + | 6.45 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24501 | chr17:73990812-73991094 | Colon_Crypt_2 | | SE_24501 | chr17:73991390-73992089 | Colon_Crypt_2 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 73991168 | 73991247 | | chr17 | 73991440 | 73991952 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH17I075994 | chr17 | 73990813 | 73991094 | | GH17I075995 | chr17 | 73991290 | 73995402 |
|
Enhancer Sequence | GACGGAGTCT CACTCTCTCA CTCTGTCACC CAGCCTGGAG TGCAGTGGCG TGATCTCAGC 60
TCACTGCAAC CTCCGCCTCC CAGGTTCAAG CGATTCTCCT GCCTTGGCCT CCTGAGTAGC 120
TGGGATTACA GGCGCCTGCC ACTGTGCCTG GCTAAGTTTT GTATTTTTAG TAGAGACAGG 180
GTTTCACCAT CTTGGCCAGG CTGGTCTTGA GCTCCTGACC TCATGATCCA CCTGCCTCAG 240
CTTCCCAAAG TGCTGGGATT ACAAGCGTGA GCCACCGCGC CCGGCCTGTC TTGATTATCT 300
AAGTCATACA CGCTCGTCAT TCACGGAGGG AACTCGAATC AAAGATGAGG AGGTGGGAGG 360
AGAGCATCCT GGCTGACTGT GCTCTGTCCA CCCTGACCTC TGGCCTGGGC AGAGGGGGCA 420
CCCTGTGGCT GCTTTAAACC TCCCTGTGAA AACCAAGTGT GGTGGCTCAT GCCTGTAATC 480
TCAGCAATTT GGGATGCCAA GGAAGGAGGA CTGCTTGAGA TCAGGAGTTT AAGACCAACC 540
TGGGCAACAT AGTGAGACCC CATCTTTACA AAAATTAAAA AGTTATCCAG GTGTGGTGGC 600
ACAGGCTTGT AGTCCCAGTT ACTTGAGACG CTGAGGTGGC AGGATTGCTT GAGTCCAGGA 660
GTTCAAGGTT ACAGTGAGCC AAGATTGCTC TACTGCACTC CAGCCTGGAT GACAGAGTGA 720
GACCCTGTTT CAAAAAAAAA AAAAAGGAAA AAAAAGTCCA GGTGTGGTTG CTCACACCTG 780
TAATCCCAGC ACTTTGAGAG GCTAGGGAGG GAGGATCGCT TGAGCCCAGG AGTTCAAGAC 840
CAGCCTGGGA AATGTAGCAA GAGCCTGTCT CTACAAAATA ATAAATAAGT AGAAATAAAA 900
CCATAAACCT TCCTGTGCCA GGCCCAAAGC TCTATGGGGA CACAAAGGTT GATCAGATGT 960
GAATCCTGCC CTGTGGCCAG ACTGACAGTA CTGAGGACAG GTGAGAGGTC ACCCTTCTCA 1020
AATGTTTGCC TAAGAGCTAG CTAAGAAGAC CAACAGGTGA AGACATGCTG GTGTGTGATA 1080
AAACCCATGG ACCTGACACC CGCTGGCGCC ATCCAAAGGC CCGAGGGCCC CCTGTTCTGG 1140
AACTAAGGTG TGGGGCACAG CCTTTCCCAG GCCTACTCCA GAGGCCCTCG GAGCATGCCC 1200
AGGCTGAAGG GCACTGGACC ACAGCAAACA GCAAGCAGCT GCCCACAAGC CCTTGCCATG 1260
CATCCTCTGC CTTCTGCTTT TCTCTCACTG CACCCCTGCA CTTTGCCCTC AGAAACCTTC 1320
CTTGTGTGGC TGGGCTCAGG AGCTCACTAA TCTAGCATGT TCGGAGGCTG AGGTGGGAGG 1380
ATCACTTGAA CCCAGGAGTT TGAGACCAAC CTGGGCAACG 1420
|
