| Tag | Content |
|---|
EnhancerAtlas ID | HS018-19711 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr6:31390440-31392290 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr6:31390544-31390555 | TTGACCTTGAA | - | 6.14 | | FOXC1 | MA0032.2 | chr6:31391494-31391505 | ATGTTTACATA | - | 6.32 | | Foxa2 | MA0047.2 | chr6:31391495-31391507 | TGTTTACATAGT | + | 6.22 | | IRF1 | MA0050.2 | chr6:31391338-31391359 | GAAAAGAAAGAGAAAGAAGAA | - | 7.18 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 31390489 | 31390717 | | chr6 | 31391660 | 31391714 | | chr6 | 31391340 | 31391587 |
|
Enhancer Sequence | TAGAGGGATG CAAAAAGGGA GGAGAATTGG TAAGTTAGAG TTTTTTGGCA AAGGACTGAC 60
AATGCGCCAC ATGGATAGGA CTTCTATTCC GCTAGCTGGT GCTGTTGACC TTGAAACTCC 120
ATGTGCACTC CAGACCAAGG GCAGAGAGAG ATGCTCACTG TGGCGGGTAG GGGGGATGTG 180
TTCCTAGAAA ATCACAATGA CATTCCCCTG AGCTATATCC CTGGTTACTA CAGCATTTCC 240
TGATCTTGCC TAACAGGATT ACTTCCCTGA ACTGTAAAAT TCCTGCAGCA TTGTATACAG 300
AGAAAGAATA GGAGACATGG CAATCATGGA CAAGAAAGGA GGAAATCGTG ATAGGAAAGT 360
TAGAGATCCT GTTGCCAACA CCCAGTCAGG CATTCGGAGG CTGGGGTCAG TCTAGAAGCC 420
TTTCATAATG CCACGTGGTA GCTCCATCCA GAAATCCTCA GTTGCTCCCT GACTTCTTCC 480
AGCCCCAGGT GATGGCTAGA TCCTCCATGA AAGGAAACTG GTTCAAACAC GGCCAATATG 540
CCCAGCAACC CATGGGTAAT GGGGGATTCT CCATGTTCTC CCCAGGAAGC CTGTCTCCCG 600
TCTTGTAATG CTGGGAGCCA CACTAATCAT TTTTAAATGG CTGAAGGGGA CCCAGTATTT 660
GGTTTGATTT GATTCTAAAA ATGGAGGCCA AGAGCCTCAA AATAAAAAAA CAGAGTGGAG 720
GTCTGCTCCT GTACTCACCA TTCTGATGAA TGTACCTTGG GATCCTGAAT GAGCACCAAA 780
AATAAAGCAG CACCTTTGTC TGGGGTGATA CCTGAGATGC ATTGCCTCAT GCCAAGAAAA 840
TTAAGGACAC AGACACACAC AAGGAGTGAG TTTAGGAGTA GAGGTTTAAT AGGCAAAAGA 900
AAAGAAAGAG AAAGAAGAAT AGCTCTCTCT CCTGTGAGAG AAGGGGCACG CAAGTGGGAA 960
TTCCAGCCCA TGGCAGAGTG CACTGGATTT TATACACAGG CTGAAAGAGG TGTCTGATTT 1020
GCACAGGGCC CACAGATTGG TTGGACCAGG TGTGATGTTT ACATAGTGCA TGGGGAAGCT 1080
GACCACCCCA CCCTAATCTT CTTATGCAAA TAGGCTTTCC ACTTGGCTGA CACCATGTTG 1140
TCTGCTCCCT GCTGCACACG TGGTTGGAAA GGAAAAGAGA AGATGGAGCC GCCATTTGAA 1200
CATGCCTAGT CCCAGGTAGC CTTTTCCTAT TGGCACAACT GCTGGCATTC ACTCAGGCAA 1260
GCTTCCAGCT TGCTTGTCTA TGTCTGCAGC TCAATTTTAC AGGCTGCTCT TTGTTAGAAA 1320
AGAAAATGAT TTGGGGGCTG CTTTTCATTA AAAGGAAAAC CTTACCAAGG ACTTCTTTAC 1380
TCTCACTATC TGCCTAAATA ATTTCTTTTT AACTCCTCTA TCAGTTACAA AATCAGTTTT 1440
AAAGCACATA CTGTTCTGTG ATATTGGGAT ATCTGGACAT TTTGTTGTCA TAGGAGTTTA 1500
TCCTTGCAGG TATTACCAAA CTGCTTCCTT AGCTATCAAC ATCCTAGGAC CATGGGTCAT 1560
GACAAGCAAG GAATGTACCC TGCTAGTTTA AAGATAAACT TGATTTGCGG GGAGGGGGTG 1620
GTTTTTAGTT ACATGGGTAA GTTCTTTTGT GGTGGTTTCT GAGATTTTGG TGCATCCATC 1680
ATCTGAGGAG TGTACATGTA CCCAATGTGT AGTCTTTTCT CCCGCACCAT CCTATGACCC 1740
TACCCTCTGA GTCCCCAACG TTCATTATAT CATTCTTTTG CCTTTGCATG CCCATATAAG 1800
TGAGAACACA TGACATTTAG ATTTCAATTC CTGAATTACT TCTCTTAGAA 1850
|
