| Tag | Content |
|---|
EnhancerAtlas ID | HS148-10566 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr2:216614000-216614960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2F1 | MA0017.2 | chr2:216614784-216614797 | CAAAGGTCACCAG | + | 6.21 | | ZNF263 | MA0528.1 | chr2:216614551-216614572 | GGGGGCGGAGGAGAGGGAGAG | + | 6.51 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_45570 | chr2:216611112-216617227 | Osteoblasts | | SE_55663 | chr2:216611418-216617365 | u87 | | SE_67801 | chr2:216611418-216617365 | u87 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I215747 | chr2 | 216612493 | 216617084 |
|
Enhancer Sequence | CAAGGAGAAA ACAGAACACA AAGCATTAAA CAGGCTGCCC AGTGGATGGT CAAAATAGGG 60
GACAGGTGTG AGCAGAGTTT AGCTAAGGAG CTAAAGTTCA GAGGAATGAC CTCAGGCTTA 120
GACAAACTGA AACTCAGGGC AGGGACACAA GTCAGGGTGA CAAAACACTA CCCAGTGGGA 180
TCATAGGTCA AAGCAGAAGC CCAGTTACCA GAACTGGAGC ACGAGGTCAG AGCAGGGCAG 240
CTCATCAGTG TGTAACCAAT GCTGCTGGAC TCCTCAGTTT CCCAACAAGG GACAGGTCTG 300
GTCCCACAGT CTGGAGCAGG GCTAAGGCTG CAGGCAGGGG TGAAGAACAA GGCAGCCGGG 360
GTGTGGGGAC AGGGAGTCAG TGCTCACACT GCGATCTCGC AGCCTTCTTC TCCATAGTGA 420
CACAGCCCTG GGGCCTCTGC TCAGCCCCTG AGCTTCCAAG CAGAAAGAGC TGTAGGAGAG 480
GATGAAGTAA GTCAGGGAAA CGGAGCCACC GTCATCAGCC TGGAGCCCTT GTCCTGCATG 540
GAGTGGCGCG TGGGGGCGGA GGAGAGGGAG AGCTGCTTTT GTTTGTTTAT TTCCTCATAG 600
CAACTCACAA ACTTAGCCAA ATACAGATAC AAATGAAGTG CATGAAAACT TTCCTAACTT 660
CCTGACTCAG AATCGTTACT AAATATATAG ATCAGATGTA GGCGGACGAA GGCAGAATTG 720
TAGGTTCCAC CTAACAGTCC TCAAACACTG CTGCCCCTGT GCCCCTCCAT GTAGAAAGAG 780
CTCCCAAAGG TCACCAGGAT GTGCTTGCCG TTTTGCTCAG TATTTTCTAA AATAATCAAA 840
ATGGAAACTG AAAATTCACC TTCCTCATGT CTCCTAACCT CAGAGGAGCC AAGCACAACT 900
GGAGAGGCTT GGTCGAAATT GATGATTGAT TGATTAGTTA TCCTCTCTTT AGTGCCCTCT 960
|
