| Tag | Content |
|---|
EnhancerAtlas ID | HS176-21303 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr2:105877310-105878120 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:105877856-105877866 | AATGGAAAAT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr2:105877992-105878007 | AAGGTCAGGAGTTCA | + | 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 |
| GH02I105260 | chr2 | 105877161 | 105878721 |
|
Enhancer Sequence | ACCTGTCTTT TTTGGGGAGG GCATAAAATT TGAGTTTCTG ACTATGTTTA CTCATATAAA 60
GGGAATACAT TCTTGTAAAC TGACTGAAGT CAAAGAAACT GAATCTCTTT TGAGGTGTAC 120
ATCATTATGT CTTGTAAACA ACTGAGAAAT GCTCTCCTGT ACTCTGTGTT AAGAAAGTAA 180
GTTTAGGATT TCAGTTATAT TCGTTTATAA GCTTCAGTCA ATAGCTGCCT GTAAGTCAGC 240
AACATATTAA AAAACAGTTT GGAAATAGTT GGTGGGGTTT TACCATAATG TGCTGGCTGC 300
AGAGGCGGGA GTGAGGGAGG GTAGGCCAAC TGACCACCCC AGTTCTATCA TGCACATTGC 360
TGTGGAGGTA AATCATAAAC ATGTGTGGGC AACCAGACAG AGGCAGGGGC TGGGTGAGTC 420
AGCTCAAAGC ACGTAGCGTC ATCTTAGCTC ACATTCCTGT TGAGGTCAGG TTGGGGATTG 480
GCCACCCCAG CTTCGTTGCA CACACATGGA TTCCGAAAGG GAAAAACTGA TATTTCAAGC 540
AAGACAAATG GAAAATGTTC TCTAGAGAAA GAGGAAGGAC TTGTGAAACC TAGAGCACAT 600
GAGAAAAGGC AAGGGGAGCC GGGCACAGTG GCTCAAGCCT GTAATCTCAG CACTTTGGGA 660
GGCCGAGGTA GGAGGATCAC TTAAGGTCAG GAGTTCAAGA CCAACCTGGC CAACATAGTG 720
AAACCCTATC TCTACTAAAA ATACAAAAAT TAGCTGGGCA TGATGGCATG TACCAGTAGT 780
CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 810
|
