| Tag | Content |
|---|
EnhancerAtlas ID | HS098-23691 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr17:29389790-29390810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr17:29390625-29390640 | TGACCTTTCACCTGG | - | 6.39 | | Nr2f6(var.2) | MA0728.1 | chr17:29390699-29390714 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6 | MA0677.1 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 6.17 | | Rxra | MA0512.2 | chr17:29390625-29390639 | TGACCTTTCACCTG | - | 6.19 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGGCCGAGG CTGGCAGATC ACCTGAGGTC AGGAGTTCGA GACCATCCCG GCCAACAAGG 60
TGAAACCCTG TCTCTACTAA AAATACAAAA ATTAACTGGG CATGGTGGCA TGAGCCTGTA 120
ATCCCAGCTA CCCAGGAGGC TGAGGCAGGA GAATCTCTGG AACCCAGGAG GCAGAGGCTA 180
CAGTGAGCTG AGATTGCGCC ACTGCACCCC AGCCTGGGTG ACAGGGCAAG ACTCCATCTC 240
AAAAAAAAAA AAAAAAGAAT CCATGTGCAT TGGAAGGATC TGGCCAAGGC ATGCTGGTAG 300
GTTTTTTCCT GCTCAAAGAT GATTATCTTG TATTCTGCTC CTTGGGCCCC TGTCTCTATT 360
GGTTTTTGGC CCATATAGTT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT CTCTCTCTCT 420
TTCTCTCTCT GTGTGTGTGT GTTTGATGGC AAATTTCAAA TATACAGTAC ATTATTATCA 480
ATCATAGTCC CCATACTGTA CAGCTTATCC CTATCGTCAT TCTTCACCTT CTAATAATGT 540
TTGTTGCTTC TTACATATTT TGAAGCCTCA TAGAAACTTG AAACTATTTA ATTCAAAGTG 600
GCCTCTTAGT CTCTTTTCTG CTTACGATAA TCGGAGTGGT TTTCTGCTGC TTGCAACCAA 660
CAATTGACTA TATAGACATG TTTGGGAGGC ATAATATAAT GCTGATTTTT TAGGTGTTGT 720
AGGGATACCA AGATGAATGC AGTCTGGAAT GCACTACACA CAGCGCATGA GAATACGGGC 780
TCCGTAGTGA GACAGGCTTC AGTTCACCTC TTGCCTCTGC CACTTACTAG CTGGGTGACC 840
TTTCACCTGG TCTTTTATCA TTGCTGGGTT TCATTTCCTC GTCTGTAAAA TGGAGTTACT 900
AAATGGTCTT GAACTCCTGA CCTCAGGTGA TCCACCCGCC TCAGCCTCCC AAAGTGCTGG 960
GATTACAGGC GTGAGCCACC GCTCCTGGCC TTGATAATGA TTCTTAACTT CAAGGAATTT 1020
|
