| Tag | Content |
|---|
EnhancerAtlas ID | HS019-02513 |
Organism | Homo sapiens |
Tissue/cell | CD20+ |
Coordinate | chr10:130135620-130137400 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BCL6B | MA0731.1 | chr10:130137311-130137328 | GGTATTTCTGGAAAGCA | - | 6.19 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH10I128337 | chr10 | 130135553 | 130136466 | | GH10I128338 | chr10 | 130137058 | 130137388 |
|
Enhancer Sequence | TTGCTTTGTT TCCTTCTTGA AGGACATTCC AATACTCTAT GCCTTCTGGA CACACACTTG 60
AGGGGCAGAA ATAGAGTCTG TACCGGCAGT GGGAATAGAA TCACCTCTTC CACATTTGTA 120
AACTTGGCTC CTTAGCATCT TGTCCCTTTG TTCTACTAAG AGAAAATGAT GAAGAAGGAG 180
TATTAGAACG AAGCTGGTAA AAAGAAGGGA AATATAAACA CACCAAGAAC CATAGGTACT 240
GAAATCTAAT TGGCCTAGTT ATTTCCAGTT ATTTTAGAAA TGACTGGGGA ATAGACTACT 300
ACTGCTTAAA AATTGCTTTA GGATTGAAGC TAGTATATTA AGCTCTTGTT TGCAGTGGCT 360
GCCTCTACAA TCACTTGTGT TCCTAAATTT GTTCAGGGCC AGGGCTATCC AGAAACCCAG 420
TGTGCACTGA CTGACCTAAC AAAGGAAGCT GCCCTGGTGC CTGTCACCAG GAAAAACACT 480
GTGTTGGTGT CAGTGCACCC CTCCAGAGAT GGTGCTTGTG TCCCTTCCAC TGAGAGCAGC 540
AAAAGCATGG GGCCCAGCCC TTCTCCTGGC ATGAACCATC CTCTCTCCGG AAAGGAGCCT 600
AGCCCAGAGC TGTCCTGGGA GCATACCATG TTTTATTACC TCTCCAGCTT CTGGTTGCCT 660
GCCAGGAGCC GAACCAGAGG TGCCAAAATG CTGTAAGAAA TCAGATCTCC AAGAGTGCCT 720
GCTCTCACGG CATTTGCAGC TGTTGGCTCA TAGCAAAGCT CTTTTTGAAT TTTGTAAGAA 780
AACATGTTCT CAAGAGGTTT CCATTCCAAG TTGGCAGGCT CAAGAAGTCA GAAGAGCTGG 840
AGTCAAAACT TTTCAAGGAA CGTCTGAGCT TGGATCCTAT TCTGCACTTA GTCCGGTCTC 900
CAACTTCTGG GGCCTCAGAT TTGGAATCGC TGTTGCTGGC TGATAATGGA CTATATTTAT 960
GGTGCCCGAG GGGAGGGTGG AGGCATGTTG CTCCCAGAAT ACCTTCAATG GTTTCAAAGG 1020
CTGTGATGCA TGGGCAGGAG ATGATTTATG GAAGCATGTT CAGGGAACAG TTTATGAGTA 1080
TCATTTGAAC ACAAATATTT GTCTTTCTTC TGGAAAAGTA GCATCTTTTC ATTCAGAAAT 1140
TAGTAGCGAA AATTCTGTTT AGCATATCCA ATTTAAGTCG TCTTTGCTCC CTCAAGAAGG 1200
TTTCCCCAAA TTATTGCAGT AATCTTTTTT TCTTCTCTCC TGACCTGTCC AATTCCAAAT 1260
TTCTGATCTG ACGGCTAAAC ACTCCCACAA AGCTGTGTTC ATCCTTAGTG AAGACCTGAT 1320
CTTTTGTCCT AGTAATTTTC ATGGGCAATT TGTCATCTTT CTGTCACTTT CCCAGTTTCC 1380
TTGCACCTTG CTGATGGTGG GTTGATAGTG ACACTATACA GAGACAGGCT GCGAATGGCA 1440
GAGAAGGCAG CTTGGGTGGA AGAAAAATGC AATTTCTCCT TGTTCAACCA ACCATTGAAA 1500
TGGCCGTTTG GCCAGAATGG TGGTGGATAT CCACATATGT TGTTTTTATT ATTGTGCTAA 1560
TGTGAGAACT GTAAATTTTT AGTGATTGGA TTTAGGAAGT TGCAAACTTG CCGTATTTAA 1620
TATTTTGGTT GAGAGAGCAT CTTCATCCAT AAAGGCAAAT ATTTTTTATG GATGGAGGCT 1680
TGTAATGATG AGGTATTTCT GGAAAGCAAT GTAGTATACT AGATTATAAA CTTCCCAAAC 1740
ATTAAAATAA AGCACTTTGG GAGGGACATT AACTCTTTTA 1780
|
