| Tag | Content |
|---|
EnhancerAtlas ID | HS043-12624 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr13:113762770-113765000 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:113763828-113763846 | CCTTCCGTCCCTTCTTCC | - | 7.12 | | ZNF263 | MA0528.1 | chr13:113764024-113764045 | CCTCCCTCTCCCGCCTGCCCC | - | 6.37 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I113108 | chr13 | 113762886 | 113766010 |
|
Enhancer Sequence | GTTCCGGAGG CGAGGGTGTC CCAGGAGCGT GGGTGTCCCG GAGGCGAGGG TGTCCCGGGA 60
GCGTGGGTGT CCCGGGGGCG TGGGTGTCCC GGGAGTGTGG GTGTCCCGGG GGAGTGGGTG 120
TCCCGGGAGT GTGGGTGTCC CGGAGGCGAG GGTGTCCCAG GAGTGTGGGT GTCCCGGGGG 180
CGTGGGTGTC CCGGGAGTGT GGGTGTTCCA GAGGCGAGGG TATCCCAGAA GTGTGAGTGT 240
CCCGGGGGTG TGGGTGTCCC GGGGGTCGTG GGTGTCCCGG GAGTGTGGGT GTTCCAGAGG 300
CGAGGGTGTC CCGGGAGTGT GGGTGTCCCA GGGGTGTGGG TGTCCCGGGG GCGTGGGTGT 360
CCCGGGAGTG TGGGTGTCCC GGGGGAGTGG GTGTCCCGGG AGTGTGGGTG TTCCGGAGGC 420
GAGGGTGTCC CGGGAGTGTG GGTGTTCCGG AGGCGAGGGT GTCCCGGGAG CGTGGGTGTC 480
CCGGGGGCGT GGGTGTCCCG GGAGCGTGGG TGTCCCAGGG GTGTGGGTGT CCCGGGGGCG 540
TGGGTGTCCC GGGAGTGTGG GTGTCCCGGG GGAGTGGATG TCCCGGGAGT GTGGGTGTTC 600
CGGAGGCGAG GGTGTCCCGG GAGTGTGGGT GTTCCGGAGG CGAGGGTGTC CCGGGAGTGT 660
GGGTGTCCCG GGGGCGTGGG TGTCCCGGGA GTGTGGGTGT CCCGGGGGCG TGGGTATCCC 720
AGAAGTGTGA GTGTCCCAGG GGCGTGGGTG TCCGGGGGGC GTGGGTGTCC CGGGGGTGTG 780
GGTGTCCCGG GGGTCGTGGG TGTCCCGGGA GCGTGGGTGT CGGGGACTGC AGGGACATGG 840
GCCTCCCCTC CCACTCCTGC CGCCCAGGGC ACCTCCTGTG AGGACTCGGA GTCCGTGAGT 900
TCCCACCTCC TTGAGCCCGA TTCTTTGGTG TCCCCGCCTG CATCCTCAGC CTCCTTCCAA 960
ACCAGACCAG TTCTCTAGGG GCGTCGACGT GTGAAACTGA TTTTAAAGAA AACAGGCAGT 1020
GGCCTTTCTC TCGGCCCCAC GTGGCCCAGT AGCGCTCACC TTCCGTCCCT TCTTCCGCGC 1080
TCAGTAACCA ATTTAGGCCG CTCCTGCAGA ACTCGGGCTC CTGCCCACCG GCCCACAGCG 1140
TCCACCTGAG GCCTCGTCCT CCCAGCAAAG GTCGTCCCTC CGGAACGCGC CTCCTGCGGC 1200
CTCTCCAGAG CCCCTCCCGC GCGTCCTCTC AGCCCCGCTC GCCTCCTCCC GGGGCCTCCC 1260
TCTCCCGCCT GCCCCCAGGC CCGTCTCCCC TCGCGGGCTG AGGCAGGTTC GGGCAGCACG 1320
GCCGCCCCGG GGCGGGGGTC ACTCTCCACC ACCGCGTGGT GCCCACAGCT CACGGCGCTC 1380
CCGGGTGACG GTCCCCTCGG CTGTAGGGCG TCCTGAAGAG CGGCCTGCTC GGAGCTGAGC 1440
GCACGGGGTT GCCTCGCCCT GGGCGTCTCT GGCCCTCACC AGCCCCGTCT TCCCATGGGC 1500
AAAACGGCGG TCCTGTTTGT CCACAAGTAA CCGTCGGGGT TACGGAGGGG CCAGGAGCTG 1560
CGGCGGGGGG CTGTGCTCTC AGGACCGGCC CCAGGAGGAT CCGCGCGAGG TCTGGAGCTC 1620
TCAGGGGTCG CGGGGGACAG AGGGGCCCCA AGCGGAGGCG GGGAAGGCGG CAGAAGCCCA 1680
GGACCGCCAA GAGCTGGCGA GGAAGCCCGG GGCTCGCTGT CGGGGGAGCC GGGCAGGGGC 1740
CGCGCCTCGG ACCAGGACGG AGGCCTGGGG AAGGCGGATC TGGCCGCCGG AGACGCGGTG 1800
CGGGTGGAGA CGAGGGATTT GGATTTCCGC GGGCGGCTGT ACGGATTTCC ACGCGCGGTT 1860
CACGTGGGCC CCAGGGGGTT GCCCGGCACC CGGGGCCGCG CCGCCTTCTC CTCGCCGGCA 1920
TCGACCCGCA GCCTCACGTT TACGCGGCGG CGCCCGCAGC CCCCTTCGGC CCGGCTTCCG 1980
CGCGTGCCCC CGAGCGCGCC CTCGGGATCA GCCCCCGGAA GCAGAGAGGC CAGGCCGGGA 2040
AGGATGGGCG ACGGGGGTGG CTGACCCGGG AGCACGGCAG GGAGGACACC CAGCCAGGCC 2100
CGCGAGCAGC GCCGCTCCCC TCCTCCAGGA CGGGCGGGAA CCTGCGATGC CCCCGCCGCG 2160
TGGGCCGTGG GGCGGTCTCC GAGGCACTGG GCGGGGCACG CGGTGGGCGC TTCACGGAAC 2220
TCGCATTTCC 2230
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