| Tag | Content |
|---|
EnhancerAtlas ID | HS061-04890 |
Organism | Homo sapiens |
Tissue/cell | GM12892 |
Coordinate | chr11:118565860-118568090 |
SNPs | | Number: 2 | 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 | CAGAGTCTCG CCCTGTCTCC CAGGCTGGAG TACAGTGGCG TGATCTGGGC TCACTGCAAC 60
CTCCACCTCC CGGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCGAGTAGC TGGGACTATA 120
GGCATGCGCC ATGACACCCG GCTAATTTCT GTATTTTTAG TAGAGATGGC GTTTCACCAT 180
GTTGGCCAGG CTGGTCTTGA ACTCCTGACC ACAGGTGATC CACCCACCTT GGCCTCCCAA 240
AGTGCTGGGA TTACAGGTGT GAGCCACCGC GCCCGGACAT TTTTGAGAAT TTTTAAAAAG 300
AGTCTATCAG AACCGAGCTC GGTGGCTTAT ATCTGTACTC CCAGCACTTT AGGAGGCCTA 360
CCTAGGTGGG TGGATCATCT GAGGTCAGGA GTTTGAAACC ATCTTGGCCA ACATGGTGAA 420
ACCCCGTCTC TACTAAAAAT ACAAAAATTA GCCGGCTGTG GTGGCGGGTG CCTGTAGTCC 480
CAGCTACTGG GGAGGTTGAG GCAACAGAGC GAGACTCTGT CTTAAAAAAA AAAAAAAAGT 540
TCACCACCAT GCTTGGTTTG GCCCCATTTG GACGGGAGGG GAGAGCAGTG AAGCAGCCGG 600
CACGTGAGGT GGCCTCCCGG GGCAGCAGAG CTGGCAGGGC AGGGCGGGCC AGGCCGGAGG 660
GCTCTGACTG ATCCTTGGAG CTCTAATAGG AAGCTGCACA CCCATTCACT CTCTTAGAAT 720
AGCTGTGCAC CTGCAGATAA CCAGTTTCTG TTGTGGTGAG TGGTAGTTAA ATAAATAAAT 780
AAGCAGGCAA AGAACAGGCT TGTCCTTACT GTGACAGTCA TTTGCTGCTG TGAAACTACT 840
ATGGTCTAAC ACCTCCCACT CACTTTCCTC AATCAGTGCT GCCTGCAATG GCAGGAACTC 900
GGGGCCAAAA GAGCACCTGC CCTAGCTCAG AGCTCGGGCC TGCCCACCCC ACCACCCCAC 960
CCCCTGGGAC CACCTGACTT TGACCTCTGA GACCACATTT GGCTTGCATG CAGGCAAGTT 1020
ATATGACTTC TCTGAGCCTC AGTTTCTTCT TTGGCAAAGT GGGGATAGTA ACAGCTCTCT 1080
TCAAAAGCCA TTGTAAGAGT TGGAAATGAT AAGCCGGGCG CGGTGGCTCA TACCTGTAAT 1140
CCCAGCAGTT TGGGAGGCCA AGGCGTGTGG ATCACCTGAC CTCAGGAGTT TCAAGACCAA 1200
CCTGACCAAC ATGGTGAAAC CCCGTCTCTA CTAAAAATAC AAAACTAGCC AGCACGGTGG 1260
CTTATGCCTG TAATCCCAGC ATTTTGGGAG GCTGAGGTGG GTGGATCACC TGACCTCAGG 1320
AGTTCTGAGA CCAGCCTGAC CAACATGGTG AAACCCCGTC TCTACTAAAA ATACAAAATT 1380
AGCAGGGCAT GGTGGCACAT GCCTGTAATC CCAGCTATTT GGGAGGCTGA GGCAGGAGAA 1440
TTGCTTGAAC CTGGGAGGTG GAGGTTGTAG TGAGCTGAGA TCACGCCATT GCACTCTAGC 1500
CTGGGGAATA AGAGTGAAAC TCCATCTCAA AAAAAAGAAA AAAGGTCGGA AATGATGTAT 1560
TTTAGCCGCG CAGATAGTCA GCCATACGCC TGTTTCACTT ATGGGTAGAA ACACTGCAGT 1620
TGACTTCATT TCAGCAGCTG AGGGGCCCAG AGGACTGTGT CCTCTGCCTC ACTGTGCAGG 1680
CCTCAGTCAT GTTCCTGGCA AATATTCCAG AAGGCTCAGA GGAGGCGTGT TGAGAGTGTT 1740
GTCAGCCAAT CACCACAAAG CTGCTCCTTC AGGAGCCTTC TCACTCTGAA CCTCACATAA 1800
CACAAGCCTG TGGCTGGAGG GAGGGTGGCA GGGGCCTACC TGGGCATTAC TTCCACGCTT 1860
GCAGCCTCAG GGTAACCCTG GTGGTCAGAT AAGCAAAGAT CAGCCTCAAA GCAGCAAATA 1920
GGACCATGTC CTCTGGGGCC TTACCATGGT CCGCATGCAG TCCAGGCTTG GCTTCACCAT 1980
TTGCATGAGA GCTCAGAGGA CACCCATGGC CACAGAGGCT TAGCTCAGCC AGGGGAATGG 2040
AGACAGTCAG TAACATGGAG GTGAGATCAT AGCAAACACC TTCATCTCCG GTTCAAGGGG 2100
GAAGGGGTCA CCTGCTGGGG AAGGAGGAGG CTCTGGCAGG TGACGCTGAG CTGGAACGTC 2160
GACCACCTTC CTCACGGCCT TGGCAGTGAA TTCCAGATGC CCAGACCTCT GCAAACAACT 2220
TCCAGCAAAT 2230
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