| Tag | Content |
|---|
EnhancerAtlas ID | HS147-10206 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr11:123955980-123957050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr11:123956675-123956685 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr11:123956675-123956686 | AAGGTGTGAAA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTCATTAAGA ATCTCCTAAC TTAGCTAAGA AGGAGAGGGA ATTAAATTAC TAAAAATTAC 60
TGCTTTAGCT CTATGAGCCA GCATTGTGAT GTACTTAATA GATATTACAT CATGCTGCCA 120
ATATCCACAT GAGGGGAGGT GGGAGGTGTA TTATTCAGAA CCAAAAGGGA GGAAACTGAG 180
GCTCAGGGAG TTCAAGTAAT AGGCCAATGC CCTACAGCGA GTAAGAAGTG TTTCTGGGAA 240
TTCAACTCAG GTCTGCATTC CCCACAGTCT CTAAAGTATG CTGCTGAAGG AATTCCGTCA 300
GTAACTCACA AGCTAGAGAG AAATGAAGGA GAAATCAACT TCTCCATCGG GATTATGGAA 360
GAGACACCAT TTGAGAGCAG TCCAGATTGA AGAGTTTAGT AGAGGTTTAT CAACAATTCT 420
TGGTCCCACA GCACAGTGTG TTTGAGAAGC CACAACTCAG TTTCATACAC GGGCATGTGA 480
ACAGAAAGGC CTGCAGGATC TGGTGATAAA GATTCTTACC CGATATGCTA TAATGTTTGT 540
ACTTCATCCT CCAGGCTGTG AAGAGTCACC AGTGAGCAAT GTAATCAGAT GGTGTTTTAA 600
AAATATGTTA TAATATGAAT CAGTGTGGAC AGGCAGCTGG ACAGGGGCCA GTGTAGTGGC 660
TAGGATTCCT TTTAAGAGGA CATCAGGGTG TGATCAAGGT GTGAAACAAA GTGGGAGCAA 720
TTGATAGGGA GACTGGATGA TAATACAAAA AAAGATTCAA AAATAGAGTA ATGGAACTGA 780
ATGGATGATT GGCCGAGTGG GAGTGTGAAA AGGTAGAGGT GCGCTCTTAG TTTCTGCCTT 840
GGGCATCTCG CATGATGTAA AGTCATTATT CTAAAGATGG AAGACAGAAG GGAAATGCTC 900
ATTTACCGCA GGCAGTACCA CATCTTGAGC CTTATTAAGA GGCTCTGACA ACTGATAGAT 960
TACCTTCTTT GTAGTGTGTT CAGCATAAAG CTTAGGTTGG TACGCACTTT AGAAAGTATT 1020
TGTCATGCTT TATTATACAT ATTAGGTTGA GGTTAGGAAG AAATTTAAAC 1070
|
