| Tag | Content |
|---|
EnhancerAtlas ID | HS010-02758 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr20:17984380-17985910 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr20:17985720-17985735 | CGAACTTTTGACCTC | - | 6.4 | | RARA | MA0729.1 | chr20:17985717-17985735 | TCTCGAACTTTTGACCTC | - | 6.38 |
|
| | 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 |
| GH20I018003 | chr20 | 17984144 | 17987054 |
|
Enhancer Sequence | TTATAAAAGG AAGATATTCG AACAAAAGGC CAGTGACAAA GGCTGTGTTA TCTACAGAGA 60
TTTTCTTCCA AACAGAATCA GAAATATAGA AAATGGATAC ACTTTTTTGC GGTGTACTCC 120
AATGTTATTT AGAGCAGCAC AGCACAGTAC ATAAAATTGT CTCAAGTCGT TTAGGAAATG 180
CTGAGGCTAG ACCAGAAACA AGAGGGAGAA AATCGCCCGT TTAACAACTT TCCCCTTCAT 240
GAAGCTCGAG ACACATATAG GACATGGGGC AAAGACCTGG TGTGGCTCAG GGACTTTCCA 300
CCTCCTAGCT GTGTAACCTT GAACTCACCT GTCGACATTT GGAGGCCTGG GGATTCTCAA 360
GAAAAATGCA GTTAATGACA GCTTGCCTGC CTCACAGGGT CCCTTAAGAA CCAATTGTGA 420
GCCTACATGT CACAAGCCCT CATAGTCTGT AAAATGCTGA ATAAATAGAG CAGATTGTAA 480
GGCTATTCCC TGAGGCTAGG CATGAGGAGG TGAGCTGTGA GGAAGGGAGA ACCAGCTCAT 540
TAACCAGGGG AACAAATGAC AGTGTGATGG CATCCCTCCC ACATCCATGG GGGCCTCTAA 600
AATCAAGGAG CCAGCCAGTG GTAGGGCCTA GAGATGAGAG GACTGGTGGC CTCTCCAACT 660
GCTTTCCAGT TCCAGGACCT CCAGCTTGTC ACCAGGACAA CCAGGCAGCC CTCACTCCCT 720
GCACGGCAGC TCAGGTGTCA CCCCAGGACA TGGAATTGAT CGAGAGGCCT CTGCCCCTTC 780
CTTTGGTAGG TTTCTTTGCT GAATGCTCAA GAAGCAGCTC CCTGGTTAGG AATTCCAAGA 840
ACTTCTAACT GACAGGGAGT CCCAGCTGTC CCATCATGGA AGGCAGCCAC CATATGTGTG 900
GAGAGACTGT GAACTGTGAA CTACACTTAC GTAACCCTGA ACTCGAGTCT TGCTCACAAG 960
ACCCAGCTCA TGTTCCCTGC GCTGCGAAGC TTCCCAGGAA TGGTCCGTGG TTGTTCTGTC 1020
TACTGTTGCA TTTGACACAG GGCTCTGCCA AGGTATTCAC CACATCTGCT TGTATATCCA 1080
TCTCCCCACT AGACTCTGGG CAAGCCTCCA ACTTTCAAAT TATTATTATT TTTTTGAGAC 1140
AGTGACTTGC TCTGTTGCCC AGGCTGGAGT GCAACACTGG TGCCAACATG GCTCACTGCA 1200
GCCTCGAACT CCTGGACTCT AGTGATCCTC CCACCTCAGC CTCTTATGTA GCTGGGACTG 1260
TAGGCATGTG CTACTATGCC TGGCTGATTT TAACAGTTTT TGTAGAGACA GGGGTCTTGC 1320
AATTTTGCCT AGGCTGGTCT CGAACTTTTG ACCTCAAGTG ATCCACCCAA CTCAGCCTTC 1380
CAAAGTGCTG AGATTACATG CATGAGCCAC CGTGCCCGGC CTAAACCTCC CATTTTATGT 1440
TTCCTCTGCC CCTGGTCTAA CTCAGTGCCT GGTATGTGGC AGACACACAG GTCAGTGTTA 1500
CAAATGACCA TACCCTCACA CTCGCTGTTC 1530
|
