| Tag | Content |
|---|
EnhancerAtlas ID | HS187-23010 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr7:106408340-106409560 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr7:106408664-106408685 | TTTCACTTTCATTTTTCTGTT | + | 6.75 | | IRF1 | MA0050.2 | chr7:106408658-106408679 | CTTCTGTTTCACTTTCATTTT | + | 8.79 | | IRF2 | MA0051.1 | chr7:106408663-106408681 | GTTTCACTTTCATTTTTC | - | 6.38 | | Myod1 | MA0499.1 | chr7:106408637-106408650 | TCCAGCTGTTCCT | + | 6.09 |
|
| | 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 |
| GH07I106765 | chr7 | 106406261 | 106411934 |
|
Enhancer Sequence | ACATTTTCTT CAATCTCAGA GAAGACTTAT CAGATGAATA ATACATTATC ATTATTTTAT 60
GGAAGTTATA AGTGATTAAT TGACCATGCC CTGTTAAATT AAGTTTAGCC TAAAGCTGCC 120
TCCTTACATA TTTTTAAGTT GAGGCTAAAG GTTTCTCTGC ACATAGTGAA CTGTAACCTA 180
ACTGGATGTA TCAACAGACT GTAACTTGCT CTTGTACCCA TCACTGAGCT TCAGCCAATT 240
GCAGATGGCC AACTGTTTAA ACCACGTTCA AATAAGACAA ACATCAAGCT GTAACAATCC 300
AGCTGTTCCT ATTCCTCACT TCTGTTTCAC TTTCATTTTT CTGTTCATAA ATCCTTTTCA 360
CGTGAGTCTG TCTGAATCTA TTCTGGTTTG GGGATTGCCC AGTTCATGAA ACATTCTTTG 420
CTCAATTAAA CTCTGTTAAA TTTAGTTTGT CCAAAATTTT TCTTTTAGCA GCTGCAGATC 480
GCCCAACTCA TCGGTGGTAG GTCTAAGACT CGAGCATGGG TCTTTAAGCC TAAAGTCTAT 540
ATTCTTGCCA CATAGCCATG CTATCTTCTG ATACATGTAG CAAAACTGCT ACAGAATTGG 600
CCACCTGGAA CCAGTTAGTG GTATCCTGCT ATTAACCACA TGTATTGGTT ACCTGATGCT 660
GCCATAACAA ATCACCACAA ACTAGGTGGC TTAAAACAAC AAAAAATTAT TATCTCAGTG 720
TTGGCAGCTA GTAGTCTGCA ACTAAGGTGC TGGCAGGTTG ATGTTTTCCT CTGACGCCTC 780
TAGGGAACCT TCCTTGCCTC TTCCTAGCCT CTAGCAGTTG CTTGCCACCC TTGGTGCTCC 840
CTGGCTTCTA GATGCATCAC TGCAGTCTCC ACCTACGATC TTCTCCCTGT CTGTGTCCCT 900
GTGTCCCAAT GCTCCTCTTT TTATAAGGAT CCAGTTATAT TGAATTTAGG GCCCATTCTA 960
ATCCAGTATG ACCTCGTCTT AACTTGATTA CATCTGCAAA GACTGTATTT TCAAATAAGG 1020
TCATATTCAC AGGCTCCAGG TGAACATAAG CTGGGGAAAG GCACACATTC AACCCAGCGC 1080
ACAGCAGACG GAGAGTTTGT TCTTGGTTTG GGTTACTGAC AATTTTCCCT CAGCAGGTAA 1140
AGGAATACAT TTAGGAAATT TTTGTCCTGG ATTCCAACAA GAAAGAAGGA GGTGTCAAAT 1200
GCAGAAACAA GCAAACCTTG 1220
|
