| Tag | Content |
|---|
EnhancerAtlas ID | HS176-10101 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr12:90124720-90125820 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GSC | MA0648.1 | chr12:90125655-90125665 | GCTAATCCCC | + | 6.02 |
|
| | 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 |
| GH12I089731 | chr12 | 90124876 | 90128702 |
|
Enhancer Sequence | ATATGTAGTG TATTTAAAAG TTGTATAGAT ACAAAAATGT TTATCGTATA TGCATATGAT 60
TTCTATAATC ACTCTGTCTG AACCAAACCC TAAAGATTTA GGTAAAAATA GATCTTGCAT 120
ATAAATCTCT CTCTATTAAG GCATTTAGTC CATCTGAGGC TAAAATTGTC ACATTCAATC 180
AATACCCATT AATGGTGATT GGAAGGAAAC TGATCTGGAA AGGAGCCAAA TGACAAAATC 240
AGTTTCCAAA AAGAAACAGA GCGTTTATAA TAAATACACA AAACACAACT CAGTAAGCAT 300
CAAAAATAAT TGATGCCAAA AATGACCAAT TCAGTGAGTA ATATCTTACT CACTGATAGA 360
AAATATCGAA CTCTCATTTC CTTTGGGCCA AATTCTTAAA GCTATTTTTT GTGCCTTTCC 420
ATTTGCCCCT TGCTGACCTT TCTGTGTCAT CTTTTGAATA CTGAACACTC TCTCACTGCC 480
CAGGCTCCCT CTTCCTGGTT TACCGTGGCC CCATTTTCCA ACAGACCTAG AGTCTTCCTT 540
TCCATGCTAT AAGCCTAAAG TGGTAGGTGA TAATGTGAAT TTCAGATGCC TCAATCAGTG 600
GGACACATAT TTTTTAGTTA GAAAGCAGGC ACCCCTTTGG GTGTGTCTCA AATCATAGAA 660
CATACAGGGA ACTACCTACC TTTTTATGTG TAACACTTTC CTTCTAAAAA GACCAAATGG 720
GACATTATAT CTGAATTGCC ATTCAATTCT TTTTCTTTAT ACAAACATTT ATCTCTCTAC 780
TTGGCCCGTA AAAATAAAAA ATAAAAAGTA AGAGGATGTG TAGCAATCGG CCCCTTCACA 840
TTCTTGCCAG GATGATGATT CAGGGCCCTA ATAGGCACAT GACTTTCAGG CTTTCCCCTG 900
TGTCACTTTT CCACTGCATC TCATTTAGTG CATGTGCTAA TCCCCAAAAA TCCTAAGTGT 960
AATAATTTGT GAAATTTTCT ATGACTGTAA AGATGCATAA AGTTTTAATA CCCTCCATGG 1020
ACAAAAGTCC ATTTTCTTTT TTTTTGTTTC CTTGTTTTTG CTGATAGTAA CTTAATAAGC 1080
AAAGAGTAAA CTGTTATCCC 1100
|
