| Tag | Content |
|---|
EnhancerAtlas ID | HS060-06999 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr11:118565880-118567090 |
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 | CAGGCTGGAG TACAGTGGCG TGATCTGGGC TCACTGCAAC CTCCACCTCC CGGGTTCAAG 60
CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA GGCATGCGCC ATGACACCCG 120
GCTAATTTCT GTATTTTTAG TAGAGATGGC GTTTCACCAT GTTGGCCAGG CTGGTCTTGA 180
ACTCCTGACC ACAGGTGATC CACCCACCTT GGCCTCCCAA AGTGCTGGGA TTACAGGTGT 240
GAGCCACCGC GCCCGGACAT TTTTGAGAAT TTTTAAAAAG AGTCTATCAG AACCGAGCTC 300
GGTGGCTTAT ATCTGTACTC CCAGCACTTT AGGAGGCCTA CCTAGGTGGG TGGATCATCT 360
GAGGTCAGGA GTTTGAAACC ATCTTGGCCA ACATGGTGAA ACCCCGTCTC TACTAAAAAT 420
ACAAAAATTA GCCGGCTGTG GTGGCGGGTG CCTGTAGTCC CAGCTACTGG GGAGGTTGAG 480
GCAACAGAGC GAGACTCTGT CTTAAAAAAA AAAAAAAAGT TCACCACCAT GCTTGGTTTG 540
GCCCCATTTG GACGGGAGGG GAGAGCAGTG AAGCAGCCGG CACGTGAGGT GGCCTCCCGG 600
GGCAGCAGAG CTGGCAGGGC AGGGCGGGCC AGGCCGGAGG GCTCTGACTG ATCCTTGGAG 660
CTCTAATAGG AAGCTGCACA CCCATTCACT CTCTTAGAAT AGCTGTGCAC CTGCAGATAA 720
CCAGTTTCTG TTGTGGTGAG TGGTAGTTAA ATAAATAAAT AAGCAGGCAA AGAACAGGCT 780
TGTCCTTACT GTGACAGTCA TTTGCTGCTG TGAAACTACT ATGGTCTAAC ACCTCCCACT 840
CACTTTCCTC AATCAGTGCT GCCTGCAATG GCAGGAACTC GGGGCCAAAA GAGCACCTGC 900
CCTAGCTCAG AGCTCGGGCC TGCCCACCCC ACCACCCCAC CCCCTGGGAC CACCTGACTT 960
TGACCTCTGA GACCACATTT GGCTTGCATG CAGGCAAGTT ATATGACTTC TCTGAGCCTC 1020
AGTTTCTTCT TTGGCAAAGT GGGGATAGTA ACAGCTCTCT TCAAAAGCCA TTGTAAGAGT 1080
TGGAAATGAT AAGCCGGGCG CGGTGGCTCA TACCTGTAAT CCCAGCAGTT TGGGAGGCCA 1140
AGGCGTGTGG ATCACCTGAC CTCAGGAGTT TCAAGACCAA CCTGACCAAC ATGGTGAAAC 1200
CCCGTCTCTA 1210
|
