| Tag | Content |
|---|
EnhancerAtlas ID | HS108-05408 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr10:45960140-45962530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr10:45961310-45961325 | AGAGGTCAAAGTTCT | + | 6.1 | | Nkx2-5(var.2) | MA0503.1 | chr10:45961587-45961598 | AAGCACTCAAG | + | 6.02 | | Nr5a2 | MA0505.1 | chr10:45962460-45962475 | GATGTCAAGGCCAGC | + | 6.31 | | RORA | MA0071.1 | chr10:45962177-45962187 | ATCAAGGTCA | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I045466 | chr10 | 45962421 | 45962570 | | GH10I045459 | chr10 | 45954611 | 45961279 |
|
Enhancer Sequence | GGCACTGGCT TCCCTAGCAC TCTCTCCTAG TTCCCAAGAT CAACAAGGCT GGTAGATTTA 60
AGAGCTCTCT CCCACCTCAC AACCTCATAC ATAGTGCCAG ATGCTCCCTG AGTTCCACAA 120
AACCTCACTG CCCTGCCACA GCTCTTCACA CAAAAGGGAG TCCAGACCAC GTCACCATGG 180
GGGACACCAA TCCATAGCTC AACCAGGGGC TGAGGTAGAG CACAGAATGC TCCCAACAGA 240
TCTAATCTTG AAACTGTAAA TTAAGAAAAA TAATCAAGAA AATTTAGATT TGAAAGAAAG 300
TACAGCAAGA GGTCATGGGA TAGAACAGAG TCTCTGGGGT GGTGAATAGT CAAACTTAGA 360
GAAAAAAATC TAGGAAGGAG AGGAAGCACT GCAGTGAGGA GAGAAATGGA CAGAGAGAAA 420
TAGGGACAGT GAGTGGCACT GAGCTGAGGA TGCACCACCA CCGCTAGAGG GCCCCAGACT 480
CCCACGCCAG CCTCGGATTC CCCAGGCTCC ACAGCCCCAC AGACCTATGC GTATTCATAA 540
AAAAGCATTC TTCCCTCCTT AAGACAGTAA GCCTGAGTAA GAATCTGCTC CATGCAACCC 600
CAACAGCCCC AGGAAAACAG TGCCACGAGT CTGTTATCAC CAGAAAGGCC ATATCACCAC 660
CCACCTTCTG CAGGCCCACC TGCATGGCCC TTGGCCCTAA CTCCTTGATA CAAAGGAGCT 720
CCACCCTGGC CCACCATTCC CTGGCTGAGG CCTAGTCCCC ACTCTTTCTA AGTACCATCC 780
CCAAGGGTGC ACTCTCATCC TGGAACTCCA CCTTTGGGAC CCCCGACCCT TGGTCAACCA 840
CCAGAACAGA TAAGGCCATT GCCTGGAAAC TCCTCCTCCC CCTACCCCTC ACAGCAAATG 900
AAGCAGCCTG GAGAGAGCCA GGATGGCACT CGGATTAAGG CACCCATCGC ATGGCTGCTC 960
CCACTCCCAG TGCAGAGATT CAACAGCACT TTAATGCAAG TCCACCTGAA GAAACAAGAT 1020
CCAAGAAGCT CTCATCAGCA TGCTTCATGT GTACACTGAG ATCACGCTGT GCCACTCCAT 1080
GAGCACATCT TCGAATTCAC CAAAGAATCT ACATTTATTT TCTAACTGAA TGTGCATATG 1140
GGCATGAGGT ACACGGTCTT TAAAAGCATT AGAGGTCAAA GTTCTTAGGA ATCTTAAGTT 1200
TACTTGGACA CATGAAAATA GCATCCTTGA AATAACCCTC CCATCACTAC CTTTGTCAAT 1260
ATTCTTCCTG AAACAAAATG AAAGACATCT AGGGATGCCT GTGGACACTA TGCTGTGACA 1320
TCCCTTGCAT CTTCTAGGCC TGACTGCATA AGCCATTGTC CTTTTTCTCC AACTGCCTTA 1380
GACACTGTCC CCTCTCCAGC ATCCTCCTCT CGGGGCACCC ATCACTGGCT CCACCTGCCC 1440
CAGAGACAAG CACTCAAGGC CTTTTAGTAC AATGGGCTTT ACTGTTTATA CCACAGGGGA 1500
GCAGATTGAG AGGGTATCCA TGCTAAGGTC CCCAAACTCC TACAGTCCCC CTGTTCTCTG 1560
ACATTTAGTC CTAACACTAT TCTGGGACTG AAAGCCTTCC TGTACTTATT GCTCTCTTCT 1620
TTTATTTCTG AGGATGACCA GCTCTGTTCA ACACACATAG GCAAGGCTAA AATGTGTCAT 1680
GAAGACCAAA GCCTGATCAC GGTGTATTGC AGAGAAGTAA GCGTCTTCAT CACCTGTCCC 1740
CAGGTAGACT TTGAGGAAGA AATACCCAGC AATATCCACA TGCTTGCCCC TCATTGCTAT 1800
GAGGTCACTT CTTCCTCTGT GTTGCTGGGT CAAGCATACT CCCTGGAACT GATGAGGCAT 1860
TGAAGGAAGC CCCCTTCCTT CAAGGGATGG CAGCAGAGGA AAGTACCTAG TCACCCTCCT 1920
CCCTTTTATC TTAGTAAGAG CATGGTCCTC TTGGAACCAC GTGTACTTTC CTGTATTCTG 1980
AAGGGAAGGC AAACCCTGTT GGGAGGAGGT AAGGTCTTAT CTGGAAAATC GTGCCCAATC 2040
AAGGTCAGTG TCCTGGGTCC GGGAGGCAGG TTTCTGATGG GAAATTAAAG TTCTGAACTC 2100
CAGTACTAAA CTACAAGTAA TCCAAGTCAA AAAGTGTACT CTGGGGTAAC GATTCCATCC 2160
TTGCATGCCC ATGATGAGGA GCAAGGCCTG AAGGTAGGAG GGCAGAGCCT CGTAACAAAA 2220
CAAAGCCTGG ATCAAGGAAG CAGCCACACC AGGCACACAC ACACGTCAGG ACATGTGTTC 2280
ACTTCCCTGT GTGGTTCCCC ATGTGTGTGC ACTTGTAGCA GATGTCAAGG CCAGCATGAC 2340
AGTGACAGCG GACCCAAGGA GGAAGGGAGT TCTGGCAGGG CTGGGGAGAT 2390
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