| Tag | Content |
|---|
EnhancerAtlas ID | HS145-24628 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr7:155743990-155745130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nkx2-5(var.2) | MA0503.1 | chr7:155744998-155745009 | CTTGAGTGCTT | - | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_34499 | chr7:155742769-155747459 | HCT-116 | | SE_58199 | chr7:155744127-155745492 | VACO_9m |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH07I155949 | chr7 | 155742313 | 155747521 |
|
Enhancer Sequence | GATTTTATTG TTCCGCAGGG GTCAGAGCTA GAAGTGTTTT GTTTTCAGAT GAATCTGGAA 60
CCTAAGCCCA TTCTGTAAGG AATTGCCACT TAGTCCTACA CATTGAATGC AGAAAATTCT 120
GATGGTTTAA TGCCTCTCAT TTGGGATATC CGAAAACAAT TAGGGCTTAT CTGGATTACT 180
GCAGCGAAAC AAAAACACTC CGTGATGGCC AAGTGTGGAG CTGGGAGGAA CAAGAGGAAG 240
GAGCCGGTGA TGGCTTTGTG ACTCTTTCCC CAAATAACAT GCCCATGAAT CAGAGGCTCT 300
GGGAGAAGGC TGCTGGTGAC TCAAGGCCGG GTAACCAGCG AGCCCTGACC GTCCCTCCGT 360
GCAGGACTCG ACTCGACAAG GAATCCAGGG AATTGCTCCG ACAACATCAG GCCCGGACTC 420
TTATTTGTTT TCATGTTTGA GGGTGGATCT AAGCCCTGCA ACATCATCAA AACATTGTTT 480
TAATGCAGGT GCCGGTGCCA CACGTTAGAG GGCTTGTGCC TGCCAGCAGT GGAAAAGTAC 540
CGCCTTGAGT CACCGCGGTG CTGAAGGTCA CTGGGCCTCC TTACGCAAGC CCTGGACCCG 600
GCGCCCATGA ACTCGCTACC CTGGGCTGCG ATTGTTCTTT CTTTGGTTTC CCTGTGAGCC 660
CCAGTGACAA ACCACCGGAA CCCAGAGTGA CTCACAGACA GTGGAGTGTC AGAGCCAAAA 720
GGGGCCGTGT GAGCTTCCAA CTCGACCCAC AGCTCTGCCA GGAGAGGCAG CTGTGTCCAG 780
AGGGGCAGGG AGACCTGCCT AGTGACCTGG CTGGTTGGTG ACACAGCCAG GCCTAAGAAT 840
GGAGTCTTCT GGTGACAGTT TAGTGTGTTT GATCATGAGG AGAGCACTCA GACCCCACAT 900
CCTCGCGGTT GTCTGTTCGT CTGGGACTCC GGGCCCCTGC CCACCTCCTC TGCTTCTCTC 960
AGTGACACCA GGTGGTTTCT TTGCCTGGGA TCCCCACACC TCCATTCTCT TGAGTGCTTG 1020
GAGCTATGAC CTGTGAGGAT CCTTAGAACT CAAGACTACT GGATGGAGAG GGGAGTGAAG 1080
GGGGCCAGCG GAAGCCTGCA GGTGCCTGGC AGGTGGGTTT CCCCTTCACT GCCTCAAGCG 1140
|
