| Tag | Content |
|---|
EnhancerAtlas ID | HS076-00195 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:3727150-3728360 |
Target genes | | Number: 11 | 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) |
| CTCF | MA0139.1 | chr1:3727626-3727645 | CACTGCCCTCTGCTGGCTG | - | 7.37 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I003811 | chr1 | 3727925 | 3728364 |
|
Enhancer Sequence | GTGAGACCCT GTCTCTGGAA TTAAAAAAAA AAGGTCCAGG CTGGGCGTAG TGGCTCACGC 60
CTGTAATCCC AGCACTTTGG GAAGCCGAGG TGGGTGGATC ACCTGAGGTT GGGAGTTCGA 120
GACCAGCCTG GCCAATATAG TAAAACCCTG TCTCTACTAA AATTACAAAA ATTAGCCAGG 180
TGTGGTGGCA GGTGCCTGTA GTCCCAGCTA CTTGGGAGGC TGAGGCAGGA GAATCCCTTG 240
AACCCGGGAG GCGGAGGTTG CAGTGAGCCG AGATTGCACC ACTGCACTCC AGCCTGGGTG 300
ACAGAGTGAG ACTCCGTCTC AAAAAAAAAA AAAAAGTTCC CCTGCCTGGC CCTGCTCCAG 360
GGCTTCATTC TCAGGAAGCA CGGATGCCCT GGGAACAGCA GAGTTTGGAA GATGCTCTGG 420
TGGGAGTTTG CAGCTGGGTG GGTGGGCAGT GGGGGCTCCC CTGCCTTCGG GCTGCCCACT 480
GCCCTCTGCT GGCTGGGCCC CACCTCAGCT GACCCTCAGA AGTGCTCCCC ATTTAGGGGC 540
AGGTGCCTGA CACCCTGAGG CCAGCTGTGC AGAGGGCTGG AAAGTGCCTA GAGTGTGTGT 600
CCTCTTCAGT GCACAGCAAA GGGACCCTCA GTTCCATTTT ACAGGTGAGG AAACTGAGGC 660
AGCGGCAAGC TGTGGTCAAA CACTCCCTGG TAACTGATCC ATCAGTGGAG TCAGGATCCC 720
CCATACTATT TTCAAGATCC AGAGAGTGCC AAGGTTCCTC TGGACCAGCA CCTTCCTCCC 780
TGCAGTCAGA GGGCAGCGGG GGCAGCTTTG TCCTGCAGCT GTGGCTGTGT GTGCCTGACC 840
GCTAACTCTC TACTCTGTTG TTGAGGATGA CAACACCGGC CTTGCATGGT TGTGGTGAGG 900
ATTCCGCGGA CCCGCCTCCG TCCCGCTGGG TAGTCTAAGG CCACACCTCC CCGCAGGGTA 960
GGCTCACAGG CTCACTGCCC GAGCCCTGGC CATTACCCTC CTCCCACGGC TCAGCCCACC 1020
CAGCTTTCCA ATCAAGGGTG CCACAGCCAC TGCCCCCGGC TTTCCTGGGC AGTAGGCAGG 1080
TGACCACCGT ACAGTGCTTA GTTGAAAAGC AAAACAGCCT TGAGGGCTGG TAAAATCCCT 1140
CTTTCAAAGG GGGGAAAACC CATGAAGAGA CTAGAAAGTA TAATCCTCTA CTGGGCACAA 1200
TTAGAGAACT 1210
|
