| Tag | Content |
|---|
EnhancerAtlas ID | HS010-00198 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr1:90222800-90223910 |
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 | chr1:90223491-90223506 | CAGGGACAAAGTTCA | + | 6.12 |
|
| | 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 |
| GH01I089755 | chr1 | 90221267 | 90225158 |
|
Enhancer Sequence | GACAGCATGA CAGACGCTAC CCCAGTCCTA GGCATGCGGA CTTGCCTCGA GCACACTGTA 60
AGTGTTCAGA CAGCTTTGGA CAAATGCTGT CTTGAACTGC CAGATCGTAC CTTCGTATTT 120
AAGAGACCAT TGCTCGGCAC AACATGGCAG CTAATATTTA AAACAAATGG TAAAGAGGAA 180
AGGCAATCAT TTCCTCACTA AATGAAAAAG GAGATATGAA TCTGAGGAAC ACAATCCGGC 240
ACTGATTGAA AGTAAATTAC CAGTTGATTA GACGGCTGTA AATTCAGGGA GAGAAGCCTC 300
AACCGGCAGC TGGATTTTGT AAGGAAGAGG GCAATTAGAG AGGGCACAGG CGAGGCAGAG 360
CACAGAGAGG GCTCTGCACA GAGCAGACAG GGCAGCTTTG CAACACTAGG ATTACAAAGG 420
CAGGAAGGGG TTTGTAGGAA GTGTTCTGTG GATGGAGCCT GCAAGAAAGG GGAGCTCCCC 480
ACTCCCACTC GCCCTGCCCC ACCTCCCTAG TGAGCAGGAA GAGGTTAAAC TGCCAGTTCC 540
CTGTCTAGCA GCAGTTAGGA CGGGTGTTTG TTATTGCAAC ACAGGAAGTA TCACGATTTC 600
TCTTCCTTTT TCAGGCTGTA CTCAATCTAG AAGCTTTTTG CTTCCTATCA AAAGCCAGGG 660
ACTTGAAAAC TACTCAGGTC CCTGCAGCCC ACAGGGACAA AGTTCATGCA GATTTCAGTG 720
GGAGATGCCA TCTCCGGATA GCAACTGGGG CCAGTTTTTG CAGATGGCAA GCGCTTAAAG 780
ATGCAAGCCT CCATGATTAC CACGAACTGA GAAATCTCTG CAATTAGCAG GAGTGTAACT 840
GGAAAACCAA GGGCTCCTCT GTGCCTTACC AAAAGACATT CCCTCTTCCT CTGGCAAGTT 900
GAAGAAGATA ATTTGGCCAG CCTAGGAGGA AGTGATTGAT TGAGACAGAA ATGGTGGAGA 960
GAAGGATGAC TGTGATTTTT ACTTTGGTGA TGGGCATGAA CATAACAAAG AACAGATGGT 1020
GGATGCCTTA GTCCCACTGG TGTTATCAAT TCCGTAGCCC TGAGCCCTGC CCTGCTACAG 1080
GCTTATGTAA TTCTCAAGCA TGTGCTCTCA 1110
|
