| Tag | Content |
|---|
EnhancerAtlas ID | HS147-00569 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:17612800-17615170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:17613334-17613349 | TGGGGTCAGGGGTCA | + | 6.67 | | NR2F1 | MA0017.2 | chr1:17614474-17614487 | CACGTGACCTCTG | - | 6.04 | | Nr2f6(var.2) | MA0728.1 | chr1:17614686-17614701 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 17613600 | 17614695 | | chr1 | 17613711 | 17613962 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I017286 | chr1 | 17613436 | 17614463 |
|
Enhancer Sequence | TGCCAGCTCC TAGAGGCTGC CTACACCCCT TGGCTTCTGG GCTTTTCCTC CATCTTCAAG 60
GCCAGCAGCA TAGTAACATT TTTGTATCTT CCTCTGATGG ATTCTTCTGC TTCCTTCTTC 120
CACTTGTAAG GACCCTTGCG ATGACACTGG GCTCATCTGG ATAAGCAAGG CTCACCCACC 180
CTCTCTAGGT CAGCTGATGA GTGAACTTCA TTCAATCTGC AACCTTCATT CCCTTTTACT 240
AAGAAGGTCA TATACTCACG AGTTCTGCAG ACTCGAACGT GGAAATCTTT GGAGGACCAT 300
TTTTCTGCTG ACTACAAGCA ACCAGGCCCT GACTGCCGTT TCTGGCCTCC AAGAGTGAGA 360
CCATACCCGG TCCCCTCTGA AATCCACAGA GGCAGCAGCA GAAAGATGCA GTCAATGAAC 420
CCTCACTCTG GGACTGGTGT TCAGTTCTGG ACCCTCCGCT GGGCTGAGAT CTGGGATCCC 480
ATGGATGCAG GCTGGGTGGC TCCAAAAAGC ACTGGAAGCT GCCTCCATCA GGCCTGGGGT 540
CAGGGGTCAC CTCCGCTGGC CACTGCCTTC CCAGACAGCT GCCCATGCCA CACTGCCTGG 600
TCCCTTCCGG GGCCTGGCTC TCAGGCCTGG AAAGCCCAGG GAGACTAGGA TGAGGCTTGG 660
GTTCTCGTAG GGAAATTTCC CTTCACCCTA TTGTGGTTCC CCTAACACAG TGGGCAACCT 720
TGACCAGGCC TGAGGATAAG GGAAGATACC CAACCGACTC ACCTACTCCC AGCTGGCTGC 780
CTGAAACCCC TCGGAGTTGG ACCATCAGAT GCTGAACTCG TACTCTCTAG CTGAGCACAT 840
AACTTGGGTG AGCCTCAGTT TCCCCCTCCA TAAAATGGGC AAAATAACTG CCGCTTCATA 900
GAGCTTGCAT GGGGATGAAG TAGGGTAACT CACAAGATAT ACTTAGTGTC AATAGCACAG 960
TGCATGGTGC ATAGTAAGTG CTCAGTAAAT GATGACTGCT GTTACATAAC ATCCCCCAGC 1020
CCTTCCTCAA GCATCTGCTG TGTAGAACAC TCCTAATCTC CGCGCTTTAA TAGATGACAA 1080
AGACCCTTTG AGACCCAGAG GTGAAATGAG GGAGGTAGGG ACAGGACAGC TGTCTTGGCT 1140
ACTCTCAGAT CATACCCTGC TTGTCTCAGC TGTGTAGGAC TGGCCCAGGT GGAGGCTCCT 1200
GCCTGGACAA GAAGCTGACA AGAAAGCCTG TCTTTTTTGT GGGGATTTGC AGCTCTGGGT 1260
GGCCCTGACT CATGCTTTAT TCAGAATTTG GAATAAGTAG CTGCAGGGCT TCCGCAGGCA 1320
TTGCCCAACT CTGTGGCCTC CTGCGGCTTC CAGCAGCCCA GGAAGGAGGG CCCTGGGTGA 1380
GGATGGCTGG AAAGGAATTC TGGATGGCTG GACAGAGTCC ATGGGACCTA TCACTTCCTA 1440
CAAAGTCACT GTCATCCCAA GTCCCCTCCA GCATAATGAC GGCAAGTGCA AGCATTGTGC 1500
CAGCAGGTAC TGAATGCTTC CTGAGCACCA TCTGATATAG CCCTCACAGC ATGCCAGCAG 1560
GCAGCTATTA CTATTGTTCT CACTTTATAG ACAGGGAAAC TGAGGCACAG CCACATGAAA 1620
GCGCTTGCCC TGGTCACAGA GCTATTAAGT GGGGGAAACA AATTTGAGCC TAGACACGTG 1680
ACCTCTGTAC CCAGTCACAC CAGTGGTTCT CAACCCATCT ACACATTAGA ATCACCTGGA 1740
AGGCTCTCAT GAAAACCTAG CAGGGCCAGG CCCCCACCAT CAGAGATTCT GTCTGGACAT 1800
TGGGATGTTA CACAAAGCAA CTCGGTGACT CAGGTGTGTA GCCAGGACAC AGCAACACTT 1860
TGGAAGGCCA GGCGGGCAGA CCACCTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT 1920
GCTGAAACCC CGTCTTTACT AAAAATACAA AAATTTGGCT GGGCGTGGTG GCTCACGCCT 1980
GTAATCCCAG CACTTTGGGA GGCCGAGGTG GGCGGATCAC GAGATCAGGA GATCAACACC 2040
ATCCTGGCTA ACATGGTGAA ACCCCATCTC TACTAAAAAT ACAAAAAATT AGCTGGGCGT 2100
GGTTGCACGT GCCTGTGGTC CCAGCTACTC TGGAGGCTGA GGCAGGAGAA TTGCTTGAAC 2160
CTGGGAGGCA GAGGTTGCAG TGAGCTGAGA TCGTGCCACT GCACTCCAGC CTGGTGATGA 2220
AGCGAGATTC CGTCTCAAAA AAAAAAATTA GCTGGGTGTG GTGGCTCGCA CCTGTAATCC 2280
CAGCTAGTTG GGAGACTGAA GCAGGAGAAT CTCTTGAACC AGGGAGGCAG AGGTTGCAGT 2340
GAGCCGAGAT CGCACCACTG TACTCCAGCT 2370
|
