| Tag | Content |
|---|
EnhancerAtlas ID | HS098-03355 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:150185390-150186620 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NRF1 | MA0506.1 | chr1:150185928-150185939 | CGCGCATGCGC | - | 6.02 | | NRF1 | MA0506.1 | chr1:150185929-150185940 | GCGCATGCGCA | + | 6.32 | | SPI1 | MA0080.4 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.04 | | SPIB | MA0081.2 | chr1:150185880-150185892 | AAAGCGGAAGTA | + | 6.37 | | SPIC | MA0687.1 | chr1:150185878-150185892 | GCAAAGCGGAAGTA | + | 6.11 | | USF2 | MA0526.2 | chr1:150186010-150186026 | GGACCACGTGACTGGG | - | 6.06 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 150185878 | 150186128 | | chr1 | 150185600 | 150185848 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I150213 | chr1 | 150185372 | 150186896 |
|
Enhancer Sequence | GCAAACTTGA ACCAGACTGT GCACAAACAA GTGACAGAAG CGAAAGTGGC CTCAGCTGCA 60
AACGCAGCAC TTGATAAACC ACACTCATGA TCAGCCCTCA TTTCCACCTT AGAGAGATTG 120
AAAACATACC TAACTCCACC ATTTATAGCT GCTGAGCAGG TGGATGACAT TCGTCAACGT 180
GGGGTTTAGA ATAATGCAAT GTTTGAAATA AAATTAGAAA GAAAATAAGG CCAGGCACGG 240
TGGCTCACGC CTCGAACCCC AGCATTTTGG GAGGCCGAGG CAGGAGGATC GCTTGAGCCC 300
AAGAATTCGA GACCAACCTG GGCAACAGGA CAAGACTCCA TGTGTATTAA AAAAAAAAAA 360
TTAAGAAAAC AAAAGCTTTG TTAATCGTTA AGTAAGGATT GCAAAATGGA AGACAGTAAA 420
GAAAAGGAAG GTCCTAAGAA TCTGACCCAC GAGTTTCAGT CCAAGTAACC TGGACCTGCC 480
CAGAGGAAGC AAAGCGGAAG TAGGATCCAA AACGCTTTCA GCAGGCCGCC TGCGCCCCCG 540
CGCATGCGCA GGTCTCTGAC TTTGACCGTT TTGGCGGGTG CGCGCCAGCC CTAGTTTATC 600
TAGAGGGGAA GGGCGGTGCG GGACCACGTG ACTGGGGTTG CGGCATTTCT GGCCCAATCC 660
GAGACGGTTT CGTAGAGCGC CCTGTAGAGC AATTCGGGTT GCCCGGGTCC TTTCCGAGTC 720
TTGACCTCCT CTTTTGCTTC TGGCTTTTCG ACTCTGCTCT CGAATCTAAA AATTTGCCTT 780
GGCAGAAGTT TTTCCCTGTG TTCCAGGAAT TACATTAGGG ACACACTCTA AAGTGATCAG 840
CACTTTTTAT TTTTTTCCTT CATCAACTAA AATAACATTG CTGTCTCCCC AAGACGCTCG 900
AATTCTGTTC TATTGCTTGA GATTCCAGAA TCGCTGGAGG GCGCCCTGTT GTAAAAATAG 960
CACTCCCCAC AAAAAGAGAG AGAAAGTTTT ATCTATATCA GGGGGTTGAG GATTGGAGAA 1020
ATAAAGATGA AAAATTTAAA GAAGCAAGTG TCCCCTAGGA CTATGACAGA TACGTACCTC 1080
AACACGTACC CCCAAAGGTC ACTTTGTCAG TTTAAGCATT TAAAATCTCC CAATCTGTCT 1140
ATTCAAGCCT ATCAAAAATC TGAAGTAGTG ATGCTGAGAT AATATGTGGT TGGTCCAACC 1200
CAGTGGAGTG TGACGGGGAA ACAGGGCTTA 1230
|
