| Tag | Content |
|---|
EnhancerAtlas ID | HS073-02777 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr11:118565940-118566990 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr11:118566801-118566821 | GCCCACCCCACCACCCCACC | + | 6.13 | | RREB1 | MA0073.1 | chr11:118566804-118566824 | CACCCCACCACCCCACCCCC | + | 6.69 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I118695 | chr11 | 118566321 | 118566767 |
|
Enhancer Sequence | CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA GGCATGCGCC ATGACACCCG 60
GCTAATTTCT GTATTTTTAG TAGAGATGGC GTTTCACCAT GTTGGCCAGG CTGGTCTTGA 120
ACTCCTGACC ACAGGTGATC CACCCACCTT GGCCTCCCAA AGTGCTGGGA TTACAGGTGT 180
GAGCCACCGC GCCCGGACAT TTTTGAGAAT TTTTAAAAAG AGTCTATCAG AACCGAGCTC 240
GGTGGCTTAT ATCTGTACTC CCAGCACTTT AGGAGGCCTA CCTAGGTGGG TGGATCATCT 300
GAGGTCAGGA GTTTGAAACC ATCTTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT 360
ACAAAAATTA GCCGGCTGTG GTGGCGGGTG CCTGTAGTCC CAGCTACTGG GGAGGTTGAG 420
GCAACAGAGC GAGACTCTGT CTTAAAAAAA AAAAAAAAGT TCACCACCAT GCTTGGTTTG 480
GCCCCATTTG GACGGGAGGG GAGAGCAGTG AAGCAGCCGG CACGTGAGGT GGCCTCCCGG 540
GGCAGCAGAG CTGGCAGGGC AGGGCGGGCC AGGCCGGAGG GCTCTGACTG ATCCTTGGAG 600
CTCTAATAGG AAGCTGCACA CCCATTCACT CTCTTAGAAT AGCTGTGCAC CTGCAGATAA 660
CCAGTTTCTG TTGTGGTGAG TGGTAGTTAA ATAAATAAAT AAGCAGGCAA AGAACAGGCT 720
TGTCCTTACT GTGACAGTCA TTTGCTGCTG TGAAACTACT ATGGTCTAAC ACCTCCCACT 780
CACTTTCCTC AATCAGTGCT GCCTGCAATG GCAGGAACTC GGGGCCAAAA GAGCACCTGC 840
CCTAGCTCAG AGCTCGGGCC TGCCCACCCC ACCACCCCAC CCCCTGGGAC CACCTGACTT 900
TGACCTCTGA GACCACATTT GGCTTGCATG CAGGCAAGTT ATATGACTTC TCTGAGCCTC 960
AGTTTCTTCT TTGGCAAAGT GGGGATAGTA ACAGCTCTCT TCAAAAGCCA TTGTAAGAGT 1020
TGGAAATGAT AAGCCGGGCG CGGTGGCTCA 1050
|
