| Tag | Content |
|---|
EnhancerAtlas ID | HS105-12339 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr10:130135660-130137510 |
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 | GCCTTCTGGA CACACACTTG AGGGGCAGAA ATAGAGTCTG TACCGGCAGT GGGAATAGAA 60
TCACCTCTTC CACATTTGTA AACTTGGCTC CTTAGCATCT TGTCCCTTTG TTCTACTAAG 120
AGAAAATGAT GAAGAAGGAG TATTAGAACG AAGCTGGTAA AAAGAAGGGA AATATAAACA 180
CACCAAGAAC CATAGGTACT GAAATCTAAT TGGCCTAGTT ATTTCCAGTT ATTTTAGAAA 240
TGACTGGGGA ATAGACTACT ACTGCTTAAA AATTGCTTTA GGATTGAAGC TAGTATATTA 300
AGCTCTTGTT TGCAGTGGCT GCCTCTACAA TCACTTGTGT TCCTAAATTT GTTCAGGGCC 360
AGGGCTATCC AGAAACCCAG TGTGCACTGA CTGACCTAAC AAAGGAAGCT GCCCTGGTGC 420
CTGTCACCAG GAAAAACACT GTGTTGGTGT CAGTGCACCC CTCCAGAGAT GGTGCTTGTG 480
TCCCTTCCAC TGAGAGCAGC AAAAGCATGG GGCCCAGCCC TTCTCCTGGC ATGAACCATC 540
CTCTCTCCGG AAAGGAGCCT AGCCCAGAGC TGTCCTGGGA GCATACCATG TTTTATTACC 600
TCTCCAGCTT CTGGTTGCCT GCCAGGAGCC GAACCAGAGG TGCCAAAATG CTGTAAGAAA 660
TCAGATCTCC AAGAGTGCCT GCTCTCACGG CATTTGCAGC TGTTGGCTCA TAGCAAAGCT 720
CTTTTTGAAT TTTGTAAGAA AACATGTTCT CAAGAGGTTT CCATTCCAAG TTGGCAGGCT 780
CAAGAAGTCA GAAGAGCTGG AGTCAAAACT TTTCAAGGAA CGTCTGAGCT TGGATCCTAT 840
TCTGCACTTA GTCCGGTCTC CAACTTCTGG GGCCTCAGAT TTGGAATCGC TGTTGCTGGC 900
TGATAATGGA CTATATTTAT GGTGCCCGAG GGGAGGGTGG AGGCATGTTG CTCCCAGAAT 960
ACCTTCAATG GTTTCAAAGG CTGTGATGCA TGGGCAGGAG ATGATTTATG GAAGCATGTT 1020
CAGGGAACAG TTTATGAGTA TCATTTGAAC ACAAATATTT GTCTTTCTTC TGGAAAAGTA 1080
GCATCTTTTC ATTCAGAAAT TAGTAGCGAA AATTCTGTTT AGCATATCCA ATTTAAGTCG 1140
TCTTTGCTCC CTCAAGAAGG TTTCCCCAAA TTATTGCAGT AATCTTTTTT TCTTCTCTCC 1200
TGACCTGTCC AATTCCAAAT TTCTGATCTG ACGGCTAAAC ACTCCCACAA AGCTGTGTTC 1260
ATCCTTAGTG AAGACCTGAT CTTTTGTCCT AGTAATTTTC ATGGGCAATT TGTCATCTTT 1320
CTGTCACTTT CCCAGTTTCC TTGCACCTTG CTGATGGTGG GTTGATAGTG ACACTATACA 1380
GAGACAGGCT GCGAATGGCA GAGAAGGCAG CTTGGGTGGA AGAAAAATGC AATTTCTCCT 1440
TGTTCAACCA ACCATTGAAA TGGCCGTTTG GCCAGAATGG TGGTGGATAT CCACATATGT 1500
TGTTTTTATT ATTGTGCTAA TGTGAGAACT GTAAATTTTT AGTGATTGGA TTTAGGAAGT 1560
TGCAAACTTG CCGTATTTAA TATTTTGGTT GAGAGAGCAT CTTCATCCAT AAAGGCAAAT 1620
ATTTTTTATG GATGGAGGCT TGTAATGATG AGGTATTTCT GGAAAGCAAT GTAGTATACT 1680
AGATTATAAA CTTCCCAAAC ATTAAAATAA AGCACTTTGG GAGGGACATT AACTCTTTTA 1740
GGCCACTTAT ACAATTCCCA AAGCACCCAT CATAAATCCA GGAAATTGCA TTGTCATTGT 1800
TATACTCAGG AATAATTTCG CTCCAATACA TTTCCACATC ATACATAATT 1850
|
