| Tag | Content |
|---|
EnhancerAtlas ID | HS082-02223 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr1:160877440-160879080 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SOX10 | MA0442.2 | chr1:160878844-160878855 | TTCTTTGTTTT | - | 6.62 |
|
| | 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 |
| GH01I160908 | chr1 | 160877833 | 160878093 |
|
Enhancer Sequence | TATCCCACTT CTCCCAAACA GTATTTAAGC TCCTAGCTAA GCAAAAAACT ATTGTCTATT 60
AGCATTCAAC TGAAGAAAAG AAAGATAAAA TATTGTCTTG TTTCCATCAC TGTATTACTT 120
GGGCAACATA ATTACATAAT TCTTACCCTA AGAGAAAGCC TTCATATTTT TTTAAAAGTC 180
TTTTCAAATA AAATCTTCTT ATGTTTTAAA CAATATAAAA TACAAACTTT CACTTTATTT 240
ATTGTAAATT ATAAAGAGAT CATTGTCTTA ATATATTGTT AGCTTCAAGC TTCCTAAAAT 300
ATAAAAACAT TGTTGTCTAA AGTCACATAT TAACACTAAG CTCCGTGGTT TACAGAATCT 360
CCTACATTTT TGCAAGCTCA AGCTGATCAT TCCTTTTTTT ATCAGAACAA CCACAGTCTT 420
AAACAACAGT TTTATTTGGC GCTCACTCAA GCTCGCATGA TTATTAAAAC CTGTCCTGAC 480
TGCCAATGGC ATTCGCTCTC CCCTTTTTCG TTAGGACTTG GTGCCAACCC ACGAGGTCTG 540
GTGCCTAATG CTATCTGGCA AACTGATATT ACTCAGCATC CACCCTTTAG ATGCTTCAAA 600
TTTCTCCACG TTACTGTAGA CACTTATACA GGCCTGAAAT ATGCTACTCC TCAGACTACA 660
GAAAAAACTA AAGATGCAAT TGCTCATCTT TTTAAATCTA TTATGACTTT AGGCCTTCCA 720
CAAATTACAA AAACTGATAA TAGACATTGC TGTCTTAGTG CTCGATTTAC ATATGCATTT 780
ACAACTGTGG CACATACAAC ACAAGACTGG CATTCCTTAT AACTCAACCA GTCAGGCCAA 840
TGTTGAGCGA GCTCATCAAA CTCTTAAAGT ATATCTTAAC AAACAAAAAA GGGGGAATAT 900
TGGGCTTTCT CCTCGAGAAC AGGTAGGAGA CAACTGAACC CCTCCTGATG ATGAAAGACC 960
TGTCGTTGGA GAATCGACCA GCAATGATAG CGATGACTCG GAAGGCATCT GACATTACCT 1020
GAGGGCAGCT AAAGAAATTG GATCAACAGG CAACTATCCA GCTTGTTGCC ATGGGAGCCC 1080
CTGCAATTGC AGAGAATTGG TTTCTTATGT ATCTGGCAGT AATTGGGGGA GCTTTTGAGA 1140
AAGTAAGACA GACATGGATG CTGGGGTGGC TGGTGATTCT CATCCTTTGC CAAGTGGGAT 1200
CAGCTCAAGA ACATGTTTAC TGGAATCATA TTCTGAATCC CACTGTTGGA AATGTTATTA 1260
TGTGGTGGGA TGCTGACCCG CCTTTGTCAT CTAATGATAC TTCTTGGATG GGAGGTCGAT 1320
GGATGCCCCT GTCTTACCCC TTAACTGAAA ATTTGGGATG GATTAAACTC AATGACTCCT 1380
TGACTTTATT GTCTAGCAAC CCCCTTCTTT GTTTTTCTAC AATAGCCCAT GATAAGCACA 1440
TTACTCTTAT TCCTCTGGAG TATCTTTACT GTCACCTCAA AAGGGATGCC AAGCCCGCAA 1500
ACTTGACCTT TATTTCTGCT GTTACCATTA ATCTCACTAA GGTCTCTAAT GAAGCTACAC 1560
AAGTGCCTAG TCTTCTTATA TGCTGTCTGA GAAGGGACTG GCAATGTAAG TTTGAGGCTG 1620
TCCAGTGTGA ACCCCATGCA 1640
|
