| Tag | Content |
|---|
EnhancerAtlas ID | HS177-05842 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr12:115889760-115891330 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| INSM1 | MA0155.1 | chr12:115890854-115890866 | TGCCTGGGGGCA | + | 6.04 | | ZNF263 | MA0528.1 | chr12:115890054-115890075 | CCCTTCCTCTCCCTCTCCCTC | - | 6.3 | | ZNF263 | MA0528.1 | chr12:115890022-115890043 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | | ZNF263 | MA0528.1 | chr12:115890027-115890048 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 | | ZNF263 | MA0528.1 | chr12:115890032-115890053 | TCCCCTCCCCTCCCCTCCCCT | - | 6.91 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I115451 | chr12 | 115889005 | 115891497 |
|
Enhancer Sequence | GCGAAGGGGA GGCCGCGCCC CCGCGCCCCT CGCTCGCGCC GTGCCTGCCG CCGCCACCCG 60
CCCGGCCGCC GGGCCGGCCA CTGAGCGGCC GCTGCAGACT CGGCGGCGCC GGCGCACCTG 120
CAATCAGGCC CCGCGCCGCG CCGCCTCCTC GAGCCCAAGG CCGCCGCGCG CCGCGCTCGC 180
CGCTGATAAG AGGCGGCGGG GGAGGGGCGC AGGATGCTGG CGTTGCGGAA GGGCGGGGGA 240
TGGGTGGGCA GCTGGAGCGG GCTCCCCTCC CCTCCCCTCC CCTCCCCTCC CCTGCCCTTC 300
CTCTCCCTCT CCCTCTGCGA TGTCTCTCCC GAAAGTGTGT GACTTGCCCA TGTCTGTCTC 360
TTGTCTGCGC CTCTCCCCTA AATTCCCTCC CTCCCCAGCC CTCGCCGCGA GCGTGTGTGC 420
GCGCGTGTTC GTGTGTGTGT GCGTGTGCAT GTGTGTCTGT GTCTCCAGTT GCTCCCTGTC 480
TCCTGTACCT GTCTCTGTGC ACTTCCTGAC CTTTCTGTCT CCTACTCCCC ACCTCTCTGA 540
TTCTCTCCAC CTCCTGCTGA TTCTGTCGCT CTCTTCTCTC TTAGCATCCC CTCTTAGTTT 600
CTCCCTCTCT CCCTGTTCTA TTTCTCTCTT CCTCACCTAA CTTGGAGCCA GTCCCTCCCC 660
TCTCCCTGTG TCTGTCTTCT CTCCCTCTCT CCATCTTTCT GACTCTGACC TGCCTCTCCC 720
CTTCTCTCTC CCTTCCCTGT CTCTCCGAGT CCTTGCCTGT CCTCCTCTCT CTGCATCTTT 780
TCTTTCTGCG TCCCCAACTC CCTCTCACTT CTCCGTTCTT TCACTCATTT GTCTGTATCT 840
TCCCTTTTCT TTTCTCGCCC TGGGCTCCTC CCCATAACTC TGCGTGTCCC CTGCCCATCT 900
CAGCATCCTG TGGCACTTTC TGCATGGCCG GCCCGCCTGC AGGGACAAGG CCTTCAGAGC 960
CAGCGGTTGC AGGAATAGCT GGACCCCACA AGGGGCTAGG CTCAGCAGGT GTCCTGACTT 1020
CAGGGGGCAG GACTGTGCTC ACCTGTGCCT TTCATGTAAG GCTCTGGCGC ACTTCACAAA 1080
CAGTCATTAA GGCCTGCCTG GGGGCAGGTC AGGGAATATC ACAGCCTGGG CTGTTTGGTT 1140
ATCTTCATTA TTAATACACA CTCCCCTGCC TTAAATGAGT TTAGTGCAGG GGACAGAATC 1200
CCGACTGACG CCTGGAGAGA TTAAGGTTTC CGAGGGTTGC ACAGGCCAAA GATGACAAAC 1260
TGATACAGCA GGGATGTGAG TTTCTGCTGC TTCCTTCCTG CAGTGCAAGC CTCTGCCAGG 1320
AGCTTATAAA CCACCCTTTC TGAGACGGCT CTGGGGGTCA AGAGATGGGG CTAGATTTAT 1380
CTGAATGGGT CCTGGCCTGG TGGTCTGCTT TGCACCAAAC ATGCAAGCAG GGATCTCAGT 1440
GGAACCAGCC CCTTTTGCAC TTGAATAAAT TCAGGAGCGA TGGGAGAAGA ACAGTGACAT 1500
AGGGTTTATT TGTGTATTCA TTTTTCTGAC CAGGGGATGC ATCCAGAAAG TATCAGTAGT 1560
TAAACAACAA 1570
|
