| Tag | Content |
|---|
EnhancerAtlas ID | HS056-13386 |
Organism | Homo sapiens |
Tissue/cell | GC_B_cell |
Coordinate | chr6:40116170-40117540 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ELK4 | MA0076.2 | chr6:40117509-40117520 | GCCGGAAGTGG | - | 6.62 | | Gabpa | MA0062.2 | chr6:40117510-40117521 | CCGGAAGTGGA | + | 6.32 | | JUND(var.2) | MA0492.1 | chr6:40116422-40116437 | AAGGATGAGGTAATC | + | 6.01 | | SPIB | MA0081.2 | chr6:40116795-40116807 | AATGGGGAAGTG | + | 6.18 | | SPIB | MA0081.2 | chr6:40116814-40116826 | AATGGGGAAGTG | + | 6.18 | | ZBTB7A | MA0750.2 | chr6:40117508-40117521 | GGCCGGAAGTGGA | + | 6.24 |
|
| | 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 |
| GH06I040149 | chr6 | 40116761 | 40116890 |
|
Enhancer Sequence | TGTTTCATGG AAACACCCTA TTCTTTCAGA CTGTCAAGTA CACCTCCCAA GATGCCAAAA 60
CAAGACACAG GATCTACCAG ATGAGGGGAG AAGTGGGGTT CTTCTTCCCT TATTACATAC 120
AACAACTTTG CTGCCTTCCA AGCTTACAGT CTTTTCCATG TATCAGTCAG GGTCCCAGCA 180
GAAAACTAAA CTCAAACGGG GAAGAATTTG GTGAAGGAAA ACCTTCATGG AACATCAAGG 240
ATTAAGAGAA CAAAGGATGA GGTAATCAGG GTCTAGCAAC AAGCAGCTAC TGACGACCAC 300
GGACCAAAGG AAGGAAAAGG ATACCCAAAA CCCAATGAGG GCTGGAACTA TGGAAGAGGG 360
TCCCATCTGG TAGGACCAGA TCTGCAGAGA CACAGTTACT ATCTAAGACA CGGCTTTGAA 420
GCCAAGAGGG AGTCAGGAAT CAGAACCCAA AACTCTTTCC CACCAACCTT CTCTCCTAAT 480
CAGGGTGTCT CCAAACCTAC CTGGATATCA GTTTCCAAGG GAGACTGGGT GATGTATTCC 540
ACAAGAGTTA CCCTACTGGG GCACAGAACA AAGTGGAGAA CAGATGTTAG GGAGGGTCAG 600
AGAATAACCA GCTCATCTGG GGACAAATGG GGAAGTGAGA ATCTAATGGG GAAGTGAGAA 660
TCTGAAGGGG ATAACCTGTA CAATACTCCT AGAGGACAAG GTACAGGGGT CTGTAACCAA 720
TCTTAAGTCC CATACAGGCT GGAACAAGCC TGGACTGGAG CAGGACAAAA AAATGAACAA 780
GTTGACTTTC TCAATAACTA AGTGGGGATT CATAGCAGAA TTACTGGTTT GGAGATAGAA 840
TTCTAACATT CATCCAAAAA TATGGATTGA AATCCCAGTC ACATGGAGCT AGGAAGTCGA 900
GACCTCTCCA GCTGTGGAAT TCACCATTGT CAGCGTTTAC CTAGATGTTC TATGCATGCT 960
GCCTCCAGGC TTGGTACAGC TCCCACACAT CCTTGCTCCC CAAATGAGAT CATTTTCTTA 1020
GTCCTGTTAC CAGGGAGGTT AGTGACTTCC ATTTTCTGAT GGTGTTAGAT TGGATAATAA 1080
GTCAATCCTG ATTAAGAAGG CATTATCCTG TTAGGAGGCA CCAACATCTC AGCTTGGGGA 1140
AACTGCTGGG GATTATTTGA GAAAAGAAAG TCTAGTGACT GTTTTATACT TGAGTGTATT 1200
AAGAAAGATT ACAAGACAAT GCCTTTCTTC AACTTGCTTA GTTTAGCATA GCACTGTCTG 1260
AGGTTTGAAA ACAATGTTAA TGGTACACAA GTGTATTAGT CAACATCAGA AAGGTGTCTG 1320
GCAAAAGGGA AGGAATATGG CCGGAAGTGG ACATTGTGCA AATGTGTTTT 1370
|
