| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00135 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:3727370-3728610 |
Target genes | | Number: 13 | 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 | TGAGGCAGGA GAATCCCTTG AACCCGGGAG GCGGAGGTTG CAGTGAGCCG AGATTGCACC 60
ACTGCACTCC AGCCTGGGTG ACAGAGTGAG ACTCCGTCTC AAAAAAAAAA AAAAAGTTCC 120
CCTGCCTGGC CCTGCTCCAG GGCTTCATTC TCAGGAAGCA CGGATGCCCT GGGAACAGCA 180
GAGTTTGGAA GATGCTCTGG TGGGAGTTTG CAGCTGGGTG GGTGGGCAGT GGGGGCTCCC 240
CTGCCTTCGG GCTGCCCACT GCCCTCTGCT GGCTGGGCCC CACCTCAGCT GACCCTCAGA 300
AGTGCTCCCC ATTTAGGGGC AGGTGCCTGA CACCCTGAGG CCAGCTGTGC AGAGGGCTGG 360
AAAGTGCCTA GAGTGTGTGT CCTCTTCAGT GCACAGCAAA GGGACCCTCA GTTCCATTTT 420
ACAGGTGAGG AAACTGAGGC AGCGGCAAGC TGTGGTCAAA CACTCCCTGG TAACTGATCC 480
ATCAGTGGAG TCAGGATCCC CCATACTATT TTCAAGATCC AGAGAGTGCC AAGGTTCCTC 540
TGGACCAGCA CCTTCCTCCC TGCAGTCAGA GGGCAGCGGG GGCAGCTTTG TCCTGCAGCT 600
GTGGCTGTGT GTGCCTGACC GCTAACTCTC TACTCTGTTG TTGAGGATGA CAACACCGGC 660
CTTGCATGGT TGTGGTGAGG ATTCCGCGGA CCCGCCTCCG TCCCGCTGGG TAGTCTAAGG 720
CCACACCTCC CCGCAGGGTA GGCTCACAGG CTCACTGCCC GAGCCCTGGC CATTACCCTC 780
CTCCCACGGC TCAGCCCACC CAGCTTTCCA ATCAAGGGTG CCACAGCCAC TGCCCCCGGC 840
TTTCCTGGGC AGTAGGCAGG TGACCACCGT ACAGTGCTTA GTTGAAAAGC AAAACAGCCT 900
TGAGGGCTGG TAAAATCCCT CTTTCAAAGG GGGGAAAACC CATGAAGAGA CTAGAAAGTA 960
TAATCCTCTA CTGGGCACAA TTAGAGAACT TAGAGAACAT TCTGAATTTA TTCCACAGGA 1020
TGAAACTGGT CAATCATTTT CTCTAATCTC CATGTGGCTT CAAATTGTCC AGTTTCTTCA 1080
GCAGTGAACT TGTTTTGACA AATTACTTAT TCTAGGGACC AAACCCTCAG GGCAACTTCA 1140
TATTTGCCGT GTCTTTTTTC AGCAATTTTC AATCTACTTT CTAAGGTTTC AGGGCTGGGC 1200
TACACTTCCA TGTTTATTAA AGTAAATGTA ATTGACAAAT 1240
|
