| Tag | Content |
|---|
EnhancerAtlas ID | HS098-46637 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr5:149605460-149606680 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr5:149605526-149605541 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I150227 | chr5 | 149606628 | 149608033 |
|
Enhancer Sequence | CCATACCTGG CTAATTTTTG TATTTTTAGT AAAGATGGCG TTTCACCATG TTGGCCAGAC 60
TGGTCTTGAA CTCCTGACCT CAGGTGATCC TCCCAACCTC AACCTCCCAA AGTCCTGGGA 120
TTACAGGCGT GAGCCACCGC ACCCGGCCGA GAATTCAATC TTCCTTGTTA GCCTTGGAGA 180
ATTCATTTGA TTTATTAAAG GAAGATGTTG TTTTCTTCTT CACAACTTTT TGGAGGGTGT 240
CCTTGGCCTC TGTACTCTAC AAAGTTCAGT CAGAGAGGGT GCAAGCCAGG GTAGGAGTGT 300
CAGTCCCAGT GGGGTTTGCT AATGTGCAGA TACAGCAGGT GCTACAGGGA AGGGAAAGGG 360
CACTGGGGTG AGTCAGGTCT AGGTTCTGCC ACCGGCTTCC TGGGTTCCTT TAGACAAGTC 420
ACTTCTCTCT GAGTCTCAGT TTCCCCTCTG TATGATGAAG AGCTGGACTA GATCCTACTT 480
CAGTCACTGA AGTACCTTCT TTGTTATTTT TGCCATTCAC AAGTGCCACT GTACGTACTT 540
CATTAAAGTA TTTCCTGGGG TGGGCTTGGT GGCTAACACC TGTAATCCCA GCACTTTGGG 600
AGGCCGAGGC AGGCAGATCA CCTGAGGTCT GGAGCTTGAG ACCAGCCTGG TCAACATGGT 660
GAAACCCCGT CTCCACTAAA AATATAAAAA TTAGCCGGGT GTGTTGGCGG GCACCTGTAA 720
TCCCAGCTAC TCAGGAGGCT GAGGCAGGAG AATTGCTTGA ACCCAGGAGG CGGAGGTTGC 780
AGTGAGCCAA GATCGTGCCA CTGCACTCCA GCCTGGGCAA GAGTGAGACT CAGTCAAAAA 840
AAAAAAAGGG GGGGGGGGGA TTTTCCTGAA TTGATTGACT TTACTAATTT CTATAGGTTT 900
TTTGTTTTTT GTGTTTTTTT TGTGGAGATT GAATCTTGCT CTGTCGCCCA GGCTGGATTG 960
CAGTGGTGCG ATCTTGGCTC ACTGCAGCCT CAGCCTCCCG AGCAGCTGGG ATTACAGGCA 1020
CCCACCACCA TGGCCATCTA ATTTTTGTAT TTTTAGTAGA GATGGGGTTT CACCACATTG 1080
GCCAGGCTGG TCTCAAACTC CTGACCTCAA GTGATCTGCC CGCCTCAGCC TCCCAAAGTG 1140
CTGGGATTAC ATGCGTGAGC CACCGCGCCC GGCTATAGAT TTATTTTAAA AGAAAACTTA 1200
TTGACATAGT CATTGATGAA 1220
|
