| Tag | Content |
|---|
EnhancerAtlas ID | HS078-05702 |
Organism | Homo sapiens |
Tissue/cell | H2171 |
Coordinate | chr14:101539270-101540350 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN | MA0488.1 | chr14:101539709-101539722 | ATGACATCATTAC | - | 6.48 | | JUND(var.2) | MA0492.1 | chr14:101539708-101539723 | AATGACATCATTACC | - | 6.2 | | NR2C2 | MA0504.1 | chr14:101539588-101539603 | AGGGGGCAGAGGCCA | + | 6.05 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I101070 | chr14 | 101537262 | 101542129 |
|
Enhancer Sequence | TAAATATGTT TGTGTGTCTG TATGTTCGGA GATGATGTTT GTTAAGCGGG AGGTTTAACA 60
ACGGAGGCCA TCTGCCTTCA GCAGGGATTC GCACAGAATG TCACTGGCCT TCGCCCAACA 120
AGCACTTTGC AGGGAGCAAC CTCCTGAAGT CGGGGCTCAC TCCTGGGTCC CCCTCCACTG 180
CATGCGAGCC CCCCGTTCCA AGGCAGGAGC CAGGGTCACG AAAATGCATG CTTCTTCATC 240
AATCCGAGGT CTCAAACGGC TCCCCCAGCC CCACTGCCTG CCCGTTCCAG GCCTGGGGCT 300
GGCAGCCTGG GCCCCACGAG GGGGCAGAGG CCAGAGCCCG GCGGCAGAGC CCGTGCCCAC 360
GCCTCGCTGC TGCCAGCCTC CGCTTGGTCA CGACACAGCC AGGCTGACTC AGACACAGCC 420
CCAAGCGGGA GCCTCATAAA TGACATCATT ACCTATGAAA CCTGCCGTGT AGTGCGCTAG 480
CAGGGAAGGA CACACTCTGG CCGCCCGGTG ACTCACACTG TTTTCCCCAG AGCCTTCCTG 540
CTCCACCGCC TGGGTCTGAG CTGGCTGGGC AGGGGGAGGG GGCACTCAGC TTGGCCTCAC 600
TCCCCCGCTC TGCTGCAAAT GCAAAAGCAA TCGGCCAGGC AGCCACCATC CTGCTGAGGG 660
CTGTGTGTGG GGGTGGCGGG GAGGAGGGGG GGCACCATCT CTCCGGCCTC CCTCTGCAGC 720
CCCAGTGGCG CTCCAGAGGG ACTGTCAGTT GCCTATGACA GGGGAGGAAA CTGAGGCCTA 780
AAGAGGCCCA ATGCCTGGCC TCACAGATCC CACAGGGGAG GGTGGCTTCG GCTCATGCTG 840
GGAACCCCCA GGGAGACCCT TCGGCGAACC CAGCCGCTGG GCAAAGCTGC AAAACCTCTG 900
GCTGTTCCTG CTGGGCCTGA GACTCCAGCT TCTCCTGAGC TCCTTTGGTG CAGCCAACTC 960
CTCCTGCTGA AAAACACTTC TACTCTTGAA AGTGGTGGCC TTGCCAACCC AAGATGTCCC 1020
CACCAGGTGG GGGGCACTGT AGGGGAATGC TAGTTTTTTT TTCTTCAATT AAAAAAAAGT 1080
|
