| Tag | Content |
|---|
EnhancerAtlas ID | HS062-06812 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr17:17544770-17545850 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr17:17545301-17545320 | CAGTGCCACCTGGCGGATG | - | 6.05 | | HOXA13 | MA0650.2 | chr17:17544931-17544942 | GTTTTATTGGC | - | 6.14 | | Nkx2-5(var.2) | MA0503.1 | chr17:17545810-17545821 | CTTGAGTGCTT | - | 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 |
| GH17I017641 | chr17 | 17545201 | 17545390 |
|
Enhancer Sequence | GGGCAATCAA AGTTCCCATC ATTGGACTAA GAGGGGCAGG AACGTCCACC TGTCTTTCCT 60
CAGATAAGAG AAGGGGCTCT TGGAGACTTT GGGGGGCCAT TTAGACGTTG AGAGCTTAGT 120
TCCTACACCA CAGTTCCTAC ACCACTGATG GCTGCTGCCA TGTTTTATTG GCGACCTGCT 180
CCGGGCCAGG CACGTGGATT GTTTTTAATC ATCTCGGCAA AATCTCAAGG TGGGGCCAGT 240
CTTTGATTTA TGGAGGAGAA AACCGAGACT CTGAGAGGTG GTTTGCTCAA TGTCACACAG 300
CTGGAAGGTG GCAGAGGTGA GAGGGGCCTC TGGTCTGCAC TGACCCTTCT CATGAGGCCA 360
CATATACCCA CTACCATCTT AGCGCATGTC TCGGGGTCTG TAAGGATTTT CCACACTCGG 420
GCAGTGCACC TTCTGGCCAT TCCTGGGTCC TTGCAACACT GGTATCTCCC CAGTTCACCA 480
GTCGTTTAAA AATGCTTAAG GGAGTTCAAT TCTGCCCCAA CACCAGGCAA ACAGTGCCAC 540
CTGGCGGATG ACAAGGACAG TACAGGAATT ACCATGTGCC CTTGGGAAAC TGTCCCCAGG 600
CAGTTGTGAT TCTAGGCCAA GGGCAGAGTT GTTTTCTTTG ACTTCATAAG AGGGGCAGGA 660
GAGGAGGCCC ACTGTTACCA CAGCTGAAAA TCAGAGGGCT GGCCCTGTCT GGGTGCTTCT 720
GACAGCGAAC CCAGACTTTC TGGGTCCCCT CTATGGTATC CTGCCAAGAG ATCATCCAGC 780
TTGGGCTTAA ATACGTCCAG GGTGGGGGTC TCACTCTCCA TGTGTCTTCA TCACAAAGTT 840
CTTGCTATCT CCGTGTAACA TCTACTCTTG GCTCTTGCTC TACTTCCACG AAGAGCTCAT 900
CAACCTTTCT GCCCTCTGAC AGCCCTTTGG AGGATCCAGG GAGCTCCACT TTCTCCTCCA 960
GACTAAGCAG CCTCCATCAC TGCTCTCAGG ACAGGAATCT GGCTCTTCTC CCTGAAGTCA 1020
TGCTCCTCAG GTCTTCCTGG CTTGAGTGCT TGTGGTTGGG AAGTAGGATG GGAGGGGCAG 1080
|
