| Tag | Content |
|---|
EnhancerAtlas ID | HS176-25180 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr22:36937350-36938730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Ar | MA0007.3 | chr22:36937951-36937968 | AGGAACATGGTGTCCCA | + | 6.32 | | NR3C1 | MA0113.3 | chr22:36937951-36937968 | AGGAACATGGTGTCCCA | - | 6.34 | | NR3C1 | MA0113.3 | chr22:36937951-36937968 | AGGAACATGGTGTCCCA | + | 6.58 | | NR3C2 | MA0727.1 | chr22:36937951-36937968 | AGGAACATGGTGTCCCA | + | 6.28 | | NR3C2 | MA0727.1 | chr22:36937951-36937968 | AGGAACATGGTGTCCCA | - | 6.43 |
|
| | 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 |
| GH22I036541 | chr22 | 36937093 | 36938746 |
|
Enhancer Sequence | TTGTCCCACT TAGCGTGAAT ATTTATACAT TTTGCTGCAG AAAAATTAAA GGGTTTATGG 60
AATATTGCTC CAGAGCTCAC TGGCATGTCA CCTGATATGC GGTAGATCCA CTCGAAAACC 120
TTTCAGGAAT CCAAAGAATT CCAAGTTATA AAGCACATTG AGGCCGGATG TGGTGGCTTC 180
AGACCTGTAA TCCCAGCACT TTGGGAGCCC AAGGCGGGCA GCTCACCAGA AGTCAGTAGT 240
TTGAGACCAG CCTGGGTGAA ACCTCATCTC TACTAAAATA CAAAAATTAG CCAGGCGTGG 300
TGGTGGGTCC CTGTAATCCC AGCTACTGGG GGAGGCTGAG GCATGAGAAT CGCTTGAACC 360
CAGGAGGTGG AGGTTACAGT GAGCCAAAAT CGGGCCACTG CACTCCAGCC TGGCCGACAG 420
AGTGAAACTG TGTCTCAAAA TAAATAAAAT ATAAAATAAA ATACATAAAT TGATAAAGCA 480
CATTGAGCCG CGAGGATTTC AGATAAGAAA TTGTGGAGCT GTGCTACCTG TACCAAACTT 540
TTCTGTCTCG GTTAGGCAGA GATCACTACC CCCATTCTGC AGATGAGGAA GACTGAGGGC 600
AAGGAACATG GTGTCCCAGG TAGGACGGCA GCCATTTTAT CATCCTGTTG GAGGCTGTGC 660
CAGCAGGAAA GGAAGCTTTG GAGCCACCAG CCCACCCCAG CCTCCCAAGA ACCTTGTTGT 720
CTCAGCAAAA TTTCAGAACT AGAAAACCTG GAAAGATTAA AGCCCCAAAG AATGCCACAA 780
GTCCCCCAGG AAGAAAGGGA GGCTTTGCTG TGCGTTCCAG TGGTCGACAT TCTAAATCAT 840
TTTTTATTTC AGCTGCATGT ACACTCACCC ATCACAGGAC CAGTTCTCAG AATAGAGAGG 900
TACCTGTTGA ATCATCCACC CTACTTCCTG CCTCGTGTGG GCATGTCTCC AAGTGCTGAG 960
CCATCCGCTT CGCTGCCGTG GCCTGAGATA TATCAGGATT TGCAGGCCTG GCGACAGGAG 1020
ACAAAATAGA TTCCCATTTC CTTCAGAACC ATTTAGCTAG TTTAGAGAGT GTTTGACTGT 1080
TTCAATGGGA TGAGCAATAA CCAGGCCTCT CCTTGGCTCC TTCTCTCTGC CCCATATGTT 1140
TTCTTCTGTT GGAAGCTGGG ATTTGGGGTC TTAGGGCCAA AGATAAATAC TGATTTTGGC 1200
TCGATCTGGC CGCACAGCTG TGGGCTAGTA GGTGCCCCTC TCTGAACCTC AGGCCCCCAC 1260
TTTCTGCAGC ACAGTGTTGT TCTCATCTCT GTTTTTTTTT TTTTTTTTTT TTTTTGAGAT 1320
GGAGTCTCTC TCTGTTGCCT AGGCTGGAGT GCAGTGGTGC GATTTCAGCT CACCGCAACC 1380
|
