| Tag | Content |
|---|
EnhancerAtlas ID | HS147-25629 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr20:25845730-25847180 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:25846226-25846246 | AACCCAACCAACACCATCCC | + | 6.06 | | ZNF143 | MA0088.2 | chr20:25847163-25847179 | TTCCCACAATGCCAAG | + | 6.18 |
|
| | 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 |
| GH20I025865 | chr20 | 25846075 | 25847036 |
|
Enhancer Sequence | CAGGACCGAC GCATCTCCTC ACGTGGGCCA GGCCTTCACA CACCCAAAGC GGATCCGCGG 60
CCGCGAAAAC GATTGACAAC CGGCCTCATG ACCCAGGCAA AGATGCAGAA AGAGGCTCAC 120
CAAAGACAGG CCGCCATGCG AGAAACCGCT TTGTGGCACA CAGGGCACAT TCGGCCAAAG 180
ACACACATGG ACACGGGCAC ACACACACAA ACCCACAGAG AGAGGGAAAG AAACTCACAG 240
AGATTGAGAG ACAGAGAGAG AAGAGAGAAT GGGAGACACA CACACAGACA CACAGATACA 300
CACACACACA CACACACACA CACACACAGA CACACACACA GAGTCATACA GCAGAGGCAT 360
GAAAACACAC ACCCCCAGGC AACCCCTGAG GCTGCGGGGT TCTGCTGTCG ACCCTCTGGT 420
GAGAGAGCAC CCTAGGGGCA CGCATTCCAA CCTGTCTTCG AGATCTCTGA CGGCGGCACG 480
ACTTTTGGGG AGACTCAACC CAACCAACAC CATCCCGGCA GGCCTGAGGC TGGGATGCCG 540
TGCTGCTTCC CCAGGACTCC GCCTGGGGTT TCCTCATCCT GGTCGGCCCT TTGCGACTCC 600
TGGCATCCGG AAACCTTCCC GTCGACCCCG TGGAGAGGTC AGGCCGGAGC CTCAGAGCCC 660
CGACACACAA GCACTGGCAC AGAGGGCTCC TGCTTTGCCG AGCCTCAGAG ACTGGTTTCT 720
AAGACAACTG TGGGAAGCAC TGTGACGGGA GAAGCCGCTC GCACCTCACG CATGCGCATT 780
GGCTGGGCCG ACTCGCTCTC CGCTCCTGGC AGGCAGGCTG CGTCCTCTTT AAATAATGCC 840
ACCGCTGCGC AGCGGCTGGA TCCGGGCTCC AGTTTGGGGC GGCGTGGGAG AGGCGACCGC 900
GGGTGTCTTG TCCTGTCCCA GGGCCAAACC CCCAGGTGTC CTGTCCCCAG GACCTCCTTG 960
AGCTGACTTC CACCTTGGGA GGAAGGGGGA GCTTCAGGAC GCCTGCTGTG TTCTCAGGAC 1020
TCCCCTTCAG ATCCCATTTT GGCCCACTCC GAGTGAGATA GGATGGGCTC GCCACATCTG 1080
GTGAGGCAGG CAGGGCCTCG CTGCAGCACA GAATGATCCC ATAGGTCTCA AGGCCTAGTG 1140
TCAGCTGCAA ATTCACTGAT CCATCAGCCC TCTGCCTCCC TCCTCCTTTG AAAGAGCAGT 1200
GGCCTGCCCA GCTTCTAAAA GCCCTGGTGC TCCGGAAAGC CCACCATGCT TTACAGGACA 1260
CTTGCAGGCA GGAACCAGGG CAAATCCGAT GTGGAGACCA TGTGACCACG CGTGGCACTG 1320
GCGTATCCCA CAGCAGATGG TGTGAATGTG TGTCACCGGA GGCATACGGA GCGATGGCGA 1380
AAGAAACGGT GGTGTCCAGG CATGTGCCGG TGGAAGGGTG GAACGAGTGA ACTTTCCCAC 1440
AATGCCAAGG 1450
|
