| Tag | Content |
|---|
EnhancerAtlas ID | HS147-03364 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr1:159566730-159568960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 6.02 |
|
| | 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 |
| GH01I159596 | chr1 | 159566407 | 159569121 |
|
Enhancer Sequence | CTGCTTGGAG TTCCACTGTC ACTCTCTTTA ATCTTTGCCT ATCCAACTGG TATCTCAGTG 60
GTCTCTTAAG GCAAATTCCT TTAATTTTAG TGACACACTC ATTTCTACTC GAAACATTTG 120
CCTCATTTTC CATGATGGAC TATTTTCTAA AACACCCACA ATATTTCCTA GATTCCTAGT 180
GGCAGTTCCC TAAGTGTGCC AAAATCCCCC AGCCTGTTAG TGTTACTTGT TATTTAAGCA 240
AAATGATTCA AATCATCATT TGATACATGA TGGAAATCCC AGGCTCACTC ACCAAATTTC 300
TAGCAAATAT TGTGTGTGCT TGTAAGGGGG ATGGGAGGGC AGGAGAAGGC CTTGTATTTC 360
TTCTAGTCAT TACAAGCTAG TGGTTTTTCT TCCTCAGTCT GGAACTTACT CCTTGCACAT 420
ACCTTTTTCT GCACTGTGCC ATCATCCACT TCTCTTTACT TCCTAACTAC CACCAACTGA 480
AAATTATACA TATAAAAGCT TTAAACAAAG TCTCTTGAGG CTCTCAAGGG AGTTTACATT 540
ACAGTATAGT TCAGCAAACA ATTTTAAATC AAATAGTACA CCTCTTTATT CTTAGAATTC 600
CCTCTGCCAA AAAAGAAATC AGCTACTTTT TTTTAAATTC AAGGTCCAAC TTTCTGTTGT 660
GTTGCTGATT CTCTTCTCTC TTTTTCCAAC GACTTCCACT TCTCTCTCTA GTTTACATGT 720
CTCCAAACCT TAAGCCTCTG TTAATACTTT CACAATAAGT CAATTTTGCC AACGGTTTGC 780
CTCCCCTAGA CCATCTAGGC TGGGCCCAGA ACACCTCATC TTCACTCCCA CTGAAGTGTT 840
CCTGAAGGTC AGCTCTCACT GACCTTGATT CTGCTCCCCT ACACTGTCAC CAGAAGCTAT 900
CCACCTATGG TTCTAATTCA GTAAGTCCAA CTCTCTCACC CCCTTTTTTT GTCTCAGCTG 960
TGTGGGCTTT CCCAGGATGG CATGCAATGG GACCCCTGTG CCATGCATAT TGTAAAGGAA 1020
AATGCCTCCC TCCATGCGCT ACAAAACAGC ACATTTATGA TGGCACTTTG AAAAGATATG 1080
GGTTGTGGTG TCACATATTG ACAATTCCTT GGCCAGAGGC TTAACAGTGC CAGCAGTGCC 1140
AGAAGATTAA GAAGACAGCA AAAACAGAAA AGGGAGAAGA TGGTGAAGTA GTTATATAAC 1200
ATGAGCGAGA ATGCTCCTGA TTACAAAGCA GAGAAATTGA CTTTTTTTCT TAGTGTTTTC 1260
TATAGTCATT GCTCTATCCC TGTTCTAGAA TTCAAGTCAT GATAAGAATT TCTTCACGTT 1320
GACTTCCTGC ATTGCTTTCA GACATTGCAA TTAAAGAATG CGAAGAAAGA ACCTCACAGA 1380
GGTAACAGAG TTTGTTTTCC TGGGATTCTC CAGATTCCAC AAACATCACA TCACTCTCTT 1440
TGTGGTTTTT CTCATCCTGT ACACATTAAC TGTGGCTGGC AATGCCATCA TCATGACCAT 1500
CATCTGCATT GACCGTCACC TCCACACTCC CATGTACTTC TTCCTGAGCA TGCTGGCTAG 1560
CTCAAAGACA GTGTACACAC TGTTCATCAT TCCACAGATG CTCTCCAGCT TCGTAACCCA 1620
GACCCAGCCA ATCTCCCTAG CAGGTTGTAC CACCCAAACG TTCTTCTTTG TTACCTTGGC 1680
CATCAACAAT TGCTTCTTGC TCACAGTGAT GGGCTATGAC CACTATATGG CCATCTGCAA 1740
TCCCTTGAGA TACAGGGTCA TTACGAGCAA GAAGGTGTGT GTCCAGCTGG TGTGTGGAGC 1800
CTTTAGCATT GGCCTGGCCA TGGCAGCTGT CCAGGTAACA TCCATATTTA CCTTACCTTT 1860
TTGTCACACG GTGGTTGGTC ATTTCTTCTG TGACATCCTC CCTGTCATGA AACTCTCCTG 1920
TATTAATACC ACTATCAATG AGATAATCAA TTTTGTTGTC AGGTTATTTG TCATCCTGGT 1980
CCCCATGGGT CTGGTCTTCA TCTCCTATGT CCTCATCATC TCCACTGTCC TCAAGATTGC 2040
CTCAGCTGAG GGTTGGAAGA AGACCTTTGC CACCTGTGCC TTCCACCTCA CTGTGGTCAT 2100
TGTCCATTAT GGCTGTGCTT CCATTGCCTA CCTCATGCCC AAGTCAGAAA ACTCTATAGA 2160
ACAAGACCTC CTTCTCTCAG TGACCTAAAC CATCATCACT CCCCTGCTGA ACCCTGTTGT 2220
TTACAGCCTA 2230
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