| Tag | Content |
|---|
EnhancerAtlas ID | HS145-04991 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr11:119461180-119462360 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr11:119461266-119461280 | AAAGAATGACTCAG | + | 6.17 | | Pou2f3 | MA0627.1 | chr11:119461681-119461697 | TCTCATTAGCATAAAC | - | 6.39 | | Stat6 | MA0520.1 | chr11:119461624-119461639 | GTTTTCCTGAGAACC | + | 6.68 | | ZNF263 | MA0528.1 | chr11:119461570-119461591 | GGTGGAAGGGAGAGGGGAGGG | + | 6.48 | | ZNF263 | MA0528.1 | chr11:119461846-119461867 | GAAGAAGGAAGAGAATGGGGG | + | 6.65 | | ZNF263 | MA0528.1 | chr11:119461567-119461588 | GGAGGTGGAAGGGAGAGGGGA | + | 7.1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I119590 | chr11 | 119460780 | 119462696 |
|
Enhancer Sequence | AGTCCTGGGT GTCCTCAAGC CACTCACACT TCTGCCTGCC CAGCTATAAA TTCGGGGGTT 60
CCTCTACACC CTCATTTTGG GTTGATAAAG AATGACTCAG AGAACTCACT GGAAGCATTA 120
TATTTACAAT TACCATTTTA TTGTAAAAGA TACAAATAAA CAGCCTGATG AACATGCACA 180
CACAGCAAGG TCTGGAAGAG TCCCAAGCAC AAAAGCTTCT GTTGGAGTCA GGGTGTGCCA 240
CCCTTCTGGT ATGCCAATAT TAGTATGTTT ACCAACCAGG AAGTTCTCCA AGCCTTGTTG 300
TTCAGAGTTT CTGTTGAGGT TTCATTATGT AAGCATGATT GATTTAATCA TTGGCCATGT 360
GACTGGACTC CATCTCCATC TTTTCCTGGA GGTGGAAGGG AGAGGGGAGG GGCTGAAAGT 420
TCCAACTCTT TAATCCCTTG GTTGGTTTTC CTGAGAACCA GCCTCTGTTC TGAAACTGTC 480
TAGGGGATCT GCTGTGAGTC ATCTCATTAG CATAAACTCA GGTGTGGCTG AAAAGGGCTC 540
ATTATGAATA ACAAAAGACA TTCCTGTCAT TCAAACTTCT GAGGGTTTTT GAAGCTCTGT 600
GCCAGGAACC TGGGACAAAG ACTAAATATA TTATTTTTGA CTTTATCCCA CTTTCCTACT 660
CACAGAGAAG AAGGAAGAGA ATGGGGGAGC ATCCTGAGTG TTTCGTGACT TCATTGTGGG 720
AGGAGGCGCC GGAACTGTAT GAGTGGTTGA AGGAAAGTAT GAAGAAAACA GAATCACAGA 780
TCATCTTTAC TTAACTGGAG GTCTATCCTA CAGAAGAGGG AGCCTCTGCC AGGAGGAATT 840
TGGACCAATG AGCGAAAGTA ATGGGAAACC AGTTTTCAGC AGGAGCTGAT AGGGTGGGCT 900
GCCTTGAGAA GTAATAAGCT CCTAGAGAAT ATTTTAACAG AGCTGAATGC AAGTTCCATG 960
TGAGCATCAA CTCAGTCGGA CTTGACTTCT GCTGTGTGCC TGGGGCCTGA ATATTACCTG 1020
ACAAACAGTA GATGCTTACT AAATATTTGG TAAATATTTG TTGAATGCAC ATTTGTGGAG 1080
GAGAAGGGAA GGTAGTTTAA ATAACATGAA AACCTAGGCC CAGTCATAAG TCTTTAGTAT 1140
CCAGCCGTTG TGCTGGCTTT TGAGGCAAAA AACAAAAAAA 1180
|
