| Tag | Content |
|---|
EnhancerAtlas ID | HS147-28070 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr3:39475020-39476860 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr3:39475312-39475333 | GAATTTAAACTGAAACTGAAA | - | 6.26 | | IRF1 | MA0050.2 | chr3:39475318-39475339 | AAACTGAAACTGAAAGTTGGC | - | 7.43 | | IRF8 | MA0652.1 | chr3:39475321-39475335 | CTGAAACTGAAAGT | + | 6.44 | | IRF9 | MA0653.1 | chr3:39475320-39475335 | ACTGAAACTGAAAGT | + | 6.01 | | KLF4 | MA0039.3 | chr3:39476296-39476307 | GGAGGGTGTGG | - | 6.32 | | RREB1 | MA0073.1 | chr3:39476294-39476314 | GGGGAGGGTGTGGTTGGTGG | - | 7.31 |
|
| | 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 |
| GH03I039433 | chr3 | 39474892 | 39475491 |
|
Enhancer Sequence | GTGAGAATGC ACTGGCCCAC CTTGCCCAAA GTAACCTCCT CTCCCAGCCC ACTTGCCCTA 60
GCCCTGTCCA GACCCCATCA GCTCTTGCTT GCTGGGCATG GATTGACAAG CTGTCAGGCA 120
GGCTGAGCTG AGCTAGGGCT CATGGAGGTA GGAACTTCAG ACCCTTTCTG CCATTTTTGA 180
ATTTGGCTTT AAAGAGGCAC AAATATTGTG TTTTAACAAT TCAAATTTTC TTTCTGGCAA 240
TGATTTGCTA GCAATGTGAG TCAGCTTCCT TAAGGTCCAC TTTTCCTTTC TGGAATTTAA 300
ACTGAAACTG AAAGTTGGCA ACAGTGTCTT CCTCTCCAGG CCAATCCCTG CAGTGGGATG 360
TGGGTCTCCT TGATGACGGC CCCTCTGTCC ACACCAAAAC CCTTGCCGAC CATTGCAAAA 420
GGCTGAGAGT TTTGAATTCT CTGTCCCTAA GAAAGAAAGG AAAACAGGGA GATCTTCACG 480
ATTATAAACT GAACCCTGGA ACACCCCTCC TGTCCTTCCC CGAACAGGCC TGTGCCCCCT 540
GCTCATTCTC CAGGTGCACC CCAAATCAAG AAAGCTCAAA TTCCAGTGAT GAGACTGGGT 600
GCTTCCACTT GGAAGCTGAG AGACATCTTC TGTCTTCTGC TTCCCTGCAA GTCTTGGGCC 660
TCCAATTAGT GGAGAGGGAA AGTGTCGCAG ACGTGGGTGT GGCAGGAGCC CAGGTGGAGC 720
CTCTGGTGGA GCGGAGGAGA GAGATGATGC TGCCTTTCCC AAGAACAAGC TCACAGTGCT 780
GCCCAAAAGG CTCCTGGAGA GGTGACTTTG CCCAACAGGC CCCAAGTTGC TTACTTTCTC 840
AGTCCTCAGG TTTTCACAGG GAAGAGACCC GCCACCCTCA CTGCCCCCAC CTCACCCAGG 900
AGGACTGAGA CTTCATTTGC TCTTCTCCTC CTTCGCTGGG TCCATTCCAC AGTGCTAGTC 960
TGAGAGGTGT GGTGTTGGGG GAAGACATAA AGGAGGTGTT TAGCCTTCTG AGGTGTGGTA 1020
GGGTAGGGGT GTTGATAAAG CCAGAGCCCC TCCTGTAAGG TAGGACTGGG TTCAGGGGAC 1080
ACTGACTTGG ATTGTAATGC CTGAGGCCTC AGGGAAGGGC TCTGATCTCA GGCAAGACAG 1140
GGCTGGGCTC GGGGAGGAGC TGGATCCCTG AATTTTTGTG AGGAGATGTT TATTTCATGA 1200
ATGTGTGTGT ATGAGGTCCC TCTGTATCCC CGCCAATACT CTGGGCCTGT CTCTGTGACT 1260
CACTCATAGT AGAAGGGGAG GGTGTGGTTG GTGGGGTTTG GTTGAGCTTA CCGTGCCCCC 1320
AGGGGATGAG AGAGGCACTC TTGGGGAACC CCCAGTAGGC GGGGTGCTGG TCTCTCTCTA 1380
CCTCCTGCAT CTGCCTGGTG GTGCCTCCTC TGGATCCCCA GCATCTCCTC GTTTCTTCAG 1440
GCCTCCCCCT TCTCCCTTGA GCCCTTATGT CCCATGTGAT ATTTTAGCTA GTTCCCATCC 1500
CATCCAAGGA GGCTGCTATC TGGCTCTGGC TGGGAAATAA ACATGTGCTT TTGCTACCAA 1560
CATCAGAATT GTGTTGTTTG TCTCAAAAGA GCACCATACT GGGGCAGCAG GTGAAGCACA 1620
GGAAGTTCTG GAAAACATCA ACTGTCACAC TCATCTCCAG GGAGAATATC CTTATAGGAA 1680
CCCTGTGGAG AGGCCAGTGT GCATCTGTGA GAGGCAGGTG GGAAATTCAC AGGATCTGAG 1740
TCAGGAGAGG AGGGTGACTA CTCAGAGGGG TTCAAAGCAA CACTTGTTAT TCCTAGAGGG 1800
GTGTTTTTAA ATGTGGCAGA GAAGGCCCAG TGTGGAGGCT 1840
|
