| Tag | Content |
|---|
EnhancerAtlas ID | HS003-11711 |
Organism | Homo sapiens |
Tissue/cell | A549 |
Coordinate | chr12:110234510-110236040 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:110235177-110235192 | TGAACTCCTGACCTC | - | 6.22 | | ZNF263 | MA0528.1 | chr12:110234861-110234882 | CCTTCCTGTTACCACTCCTCC | - | 6.01 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I109798 | chr12 | 110235881 | 110235950 |
|
Enhancer Sequence | TGCACAGGGG GCCAGGAGGG TCAGGGGGCT CACACTGGAA AGACCCCCAG GGCTGGGCCC 60
AGCTCAGCAC ATGACGCCTC CCCAGAAAAC AGCTAAGCAC CGGCTGCTGG AGGACCCTTT 120
CCTCATCTTG TTTAATTCTT GCTCTTATTA TCTTGGTTTA CAGATAAAGA ATGGAGGCTG 180
GGAAAAACGA AGGGTGTTCC AGAAGCCACT TAACCAGTCA GCTGGAGCCA GACAGAACCT 240
GGATGAGCCT TCAACATCTT AATTGTAATG AATATCTTCT TCATGCCGTT AAAATAGCAA 300
TGAATCCATC TTAATGACAT GTGAATTATA ATACTGACGA TCACATGCGG TCCTTCCTGT 360
TACCACTCCT CCTTCCCTGG CTTACACACA GGGAAGCGGA GGCACAGAGA GGGGTGGGAA 420
TTGCCCAAGG TCAGGCAATG TTAGGATTTT GGGGTTTTTG TTTTGAGACA GAGTCTCTCT 480
CTGTCACCCA GGCTGGAGTG CAGTGGCGCG ATCTCAGCAC ACTGCAACCC TCTCCTCCTA 540
GGTTCAAGCA ATTCTCCTGC CTCAGCCTCC TGAGTAGCTG GGATTACAGG TGCCCACTAT 600
CACACCCAGC TAATATTTTT GTATTTTTAG TAGAGACGGG GTTTCACCAT GTTGGCCAGG 660
CTGGTCTTGA ACTCCTGACC TCAGGTGATC CGCCCACCTC GGCCTCCCAA AGTGCTGGGA 720
TTACAGGCAT GAGCCACTGT GCACAGCCAG GATTTTGGGG TTTTTTGAGA CAGGGTCTGG 780
CTCTGTTGCC CAGGCTGGAG TGCAATGGCA CTATCACAGC TCATTGCAGC CTCAACCTCC 840
TGGGCTCAAG TGCTCCTCCC ACCTCAGCCT CCCAAAGTGC TAGGATTACA GACACGAGCC 900
ACTGAGCCTA GCCAAAGCCA GGATTTAAAC TGGAGCCTTT CTACTGCCTC AGGGCCATGG 960
TATAATTGCA ATTTTAGTAA TTTTTGCTAC ATTTTTTTTT ATTTTGGTTT TTATTTATTT 1020
GGGATCTCAA ATAATCCAGG CTGGACTTAA ACGATCCTCT CACCTCAGCC TCCCAACTAG 1080
CTGGCATTAC AGACATGTAA GTGACACTTA CTGCTTCTCC CAGGCTCCTT CCTAAGAGCC 1140
TTATGTGGAT CACCGCATTT GTCACAACAC CACACCAGAG GACACTCTTA TATCCCCATT 1200
TTACAGACAA GGAAACTGAG GCACAGAAAA GGGAAATGAG ATGTCTGAGG TCACACACTG 1260
GGAAGTGGTA GCGCCAGGGC TTGGACAGGT GCTCCTGCCT CTAGCATACT CCAGACTTGG 1320
TTCCCAATCC AGCGATGGTG CCCCCCAGAG GACAATTCAG CAATGTTCTG GAGATATTTT 1380
TGGTGGTCAC AAGTGTAAGG GGAGGTGTTC CTGGCATCTG GTGGGTAGAG GCCCGGGATG 1440
CAGATCAATG TCTGGCAATA GCACAAGACG GTCCCCACCA CAAAGAGCCT GCCGCCCAAA 1500
ATAATCATGC TGAAGTTGAG AAACCCTTCT 1530
|
