| Tag | Content |
|---|
EnhancerAtlas ID | HS037-07744 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr11:134600550-134602120 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF2 | MA0051.1 | chr11:134600626-134600644 | GGAAAATGAAAGCATTAA | + | 7.2 | | NFAT5 | MA0606.1 | chr11:134600577-134600587 | ATTTTCCATT | + | 6.02 | | NFATC1 | MA0624.1 | chr11:134600577-134600587 | ATTTTCCATT | + | 6.02 | | NFATC3 | MA0625.1 | chr11:134600577-134600587 | ATTTTCCATT | + | 6.02 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I134729 | chr11 | 134599432 | 134602180 |
|
Enhancer Sequence | CTCCCAACGG TAAGGTATGT TTCCTTCATT TTCCATTCCA GCAGGATACT GCTTTTGGCT 60
TGCTGTCCAA TGCTGGGGAA AATGAAAGCA TTAACTCACA AGGCAAGTTC CAAAGGTGCA 120
GGGCGGCTTC TGGAATATAT GGCCCTGAGG GTAGCAGACA CATGGGAGGG AAGGTATGAA 180
ATCCAAATAT GGATTCTTAT GAGGAATTTC AGGTATTCTG GCAGGCTGAC AGCTGAAATA 240
TTTAATTGAA AAAATATTTC CCAGCTTCCT CAATTCACAG CACAGAGTTC TGCCCTCTCA 300
GCCTAAACAA GAGGCAGGCC CTCCTGGTGG CTGCCCCTCT CCTGAATGCC TCACAGGAGC 360
CTGTCTCAGT CTGGGGCTGT GCTGAGCTAC CTCTTAGCAG TTTCTTTAGT CATTTTAAGG 420
TAGGGTTTCC TGGGTCAGCC AGAGACGTGC ATATCTAAAA GTCTCTTATG TCTGCATGGC 480
TAAAGGCTCA TGATTTGTAA GGCTAATGAG GTTTATAGAA CATTTAACAG AGTTTTTTGA 540
AAATTTGGAA ACAATGCAGC CGTTATCTTT GAGAGCATCC TTGCCCTTGA GTTTCCCAGC 600
TGAGATCTCC TCCCTGGGGT CTGGCTTCTC TCATCTCTTT GAATTGCACA CAGGCTTCCA 660
GTGGACAGCA CCTGCTGCTC TGCCAGCCCC AGCCAAACCT CTCCTTGCTC AGTTTTATCC 720
TGTTCCTAGG AGGAAACTGG TCTTTCCTTG GCCTTAATAA AAGCCCAAAT CCATGCACTT 780
CACAAGACCA GTCCCCAGCT GGCCCTTTTC CATGGTTTAG AATCTTTGGC CAAAAGTTGA 840
CTGTGTTTGT CATCTCCTGC TGGACTGTCG GCTCTGGGGC TAGAAAAGCC TGGAGAGATG 900
GGTAAGAGCC AGGACAAAGA AACAGAAGAC TTTTCTTGCA AAGAATAAAA GGTATGTATT 960
CATTTATTTA ATAACCATTG ATGATGTGCC TGCATGGTGC TGCACATACC TTGGGGAGGA 1020
GGGGCAGAGG CTTTGCGCCT AGACGACTCA GCATGTAGCT TAACAAAGAA ATAACCTGGA 1080
GAACAATAGC CCACAGTGTG GGGCTCCGGC ATGCTGAGCA CTGGAGCTAA AGGAGCCTGG 1140
CAGGCTTCAG AAGCCGAGCT CTGAGTGCCT CTGCCTCAGA CCCGTTCCCT GCTGACGTGA 1200
GTCACAGAAG CCAGAATCCT CTTCCCCATG GCAGCCATGG AAGCAAGGAC CTCCTCTCCC 1260
ACAAAGCGAG CCCTGAAACC TAGTGAGAAA GAAAATAAAG TTTCAATCTG AGGAACATGA 1320
GAAATTATCA GGCCTTGGGA GGTGTTAAAA TGAGAGAGGA GTCATGCCGC AGGCACCTTG 1380
AGGTAAGTAA TCATTTCAAA GCCACCTGGT GTGTGGACTC AGGACTGAGT GTTGCCACCA 1440
GTAGCTATAA ATTAATCTAA CAAGAATGGC CATCCTACAC TGGACACCAT AACTCACATC 1500
CTGTCATTCA ACAATATATA ACCAATAACT AATCAATGTC ATTTCTGCAA GCCAATTAGA 1560
ATTCCTGACC 1570
|
