| Tag | Content |
|---|
EnhancerAtlas ID | HS098-47683 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr6:11814920-11816380 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| YY1 | MA0095.2 | chr6:11815281-11815293 | TCAGCCATCTTG | - | 6.04 |
|
| | 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 |
| GH06I011813 | chr6 | 11814033 | 11816296 |
|
Enhancer Sequence | ATTGGCAAAA AGCTTATAAT TCATCCAAAT GAAAGTGGCT TCCCTGGGTC TTGGATGGTT 60
ATGCAGGGTT AGAGTTAGTG TGAGAGCTAT GAGAGATGGC TAGGGTAAAG GTCAAACAAA 120
AAACACATTC CCTTGAATAA TCATGAAACT TCTGAAGCAA ATGCATATGA AGCCCCTATG 180
ATGTTCTGTA ATGTTTCTCT AAATCCCTTT TTGCTTTGGT TTTCTGCCAG AAATGGATGC 240
AGATGCATCA GCTACCTCAC AAGGAAAACC TGTTCTCACA AGTTTTATCG CACCACTTGG 300
CAGAGAAAAA GGCTTGGGTA GAGGCTGAGA ACTTTCACAT ATAACCAGAA AGCTCGGGAA 360
TTCAGCCATC TTGACTTACC ACCCACCGCT GAAAAGAAAC TTTCGCAAAC TCTCAGAGCC 420
AGGATCTAAG AGTCCCCTCC TAATCAGAAA AGGAGGAAAC TCTACAAGGT CCAACTTTCT 480
CTTTAAAGGA AATTCTGTAG ATGGCTACAA AGCCAGGTCA TTTTAGAATT TCTCACGGTA 540
ATGAGGAGCT CAAAGACTGG TTGGCATGGT TCTCTTACCT CTATCCTTTT CGTCTCTTTC 600
CTCCCAGCCT CCATTGGCCC AAGGCAAGTT CCCTCAGAAG ACTGCACTCC CAGGAAAATG 660
CCAAGCTGGA GCTGGGAGGG ATGAGGGCTG GTATAAAAAA AGGAGCAGGA AGAGCAGTTC 720
TTTCTATTTG GGCCATTCTA TGTATTTGGA AGTCCATGAG AAATATAAGA AGGGCTCACT 780
CTAAAGAGTA AACAATGTAG ATGGCAGGAT ATGTGACTGG GAATCTGCTG AGAATGTCTT 840
CACATTACTC ACAAGTTAAT AATTTCCCTA AGAGTGGGAG TTTCTTGAGG ATGTTTAGGA 900
TTTATTTTTA AGCCTTTTAG AGCTTTGGAA TAACACTCAC AGTTTCTTTT TTACTATTTT 960
CATGGTGTTC AGAGATTTCA AGCCCACATT TTAGAACCCA CCCACCTTCA ACAGATGTAG 1020
ACAAATTAGA AATACGCAGG GACCTCTCAA ACTCATTACA GAGCTTATTT GGAACATGTG 1080
AATTATATAT GCATTTTCTA CCTCATTATC TTCATGGGAC ACTGTATATT GATTTCATTG 1140
TAAATCTGCA ATGGTAGCAT CTCACTGTAT ATAACCTGCA ACTGTGTCCC CAAGCTATTA 1200
TCATTTGTGC TAATGACAAT GCTACCTCCT TTTCACAATT AGTGCTGTGG AGTATATAAG 1260
TCAAGAGGCA TTTGCTACGA ACCTACTAGG TAGATACCAA TGCACTAGGG CCTGGGAGGG 1320
AAATATGCCC TCAGAAGATT TGCCCCTCCC TGCCTGGTAA AAGAGGCTTC TGAAAAATTA 1380
TAAAGGGAGG AAAAAACCAG TGAGGAATCT GCATTTCAAT CAGATCTGCC CGTGTTTCCA 1440
GGTTACCTGA TGGGAAAACA 1460
|
