| Tag | Content |
|---|
EnhancerAtlas ID | HS050-66379 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:81289290-81290420 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr8:81290265-81290280 | AGACCACCCACATGG | + | 6.48 |
|
| | 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 |
| GH08I080376 | chr8 | 81288559 | 81290763 |
|
Enhancer Sequence | ATATAAAAAA CACAGATTGC GGTAAGCTAT GGCCTACCTT TTTCATTTTG TGGCACCCCC 60
CTCTATCCTG CTTGGTCACT GTCTCCCACG TGGTTGTCAT AAATGTTGGG TTTCTGGCCT 120
TTGATGGACA TGATGTCACC TGCAACAGTC TTCACAAAGT CTCCGAGAAG GTACTTTATT 180
TTTGCTAGTG TTGGCTCTTT CATTTATAGT TGTAGAGAAT CTAAATTAGA ATGAAAGATA 240
TGAGGGAGCC CACAGGCCCC ATATGTCTCA CAGGGCATGT TTTGGTTAGG CCTGTTGTGT 300
TTTATATGTA TGGGACCAAG TTGAATTTCT GGAGGTATGT TGTGTTTCTT CCAAAATTTT 360
CTGGAATCCC TCATTACTGT TCCACCTTTT CCTTTGATAA TTCTGCAGAG GACAAGTCCA 420
CTGGGCCACA GGTCCTCAAT GAGGTAGCTG TTTCTAGGAG GTTAAGCAAA ATTTCTGGTT 480
AAAATGAAAC TCTTACATCT GCTCACTCAG CTGTATCACT TCAAAGAGGA AAGCAAATAA 540
AACCCAGCTT CCTGTCAGCT CCCGGCATTA AAGGATGACA AGCTACAGTT GCTTTCCATT 600
TTGACTAGAA GCAAAACTAC AGATGAATAA CATCATAGAT CAAGAAGCCA AACAAACTGA 660
AGTAACCTCT TCATCAGCAG AAATCAAGTA GTTAAAGGCA GAGTGAAAAC CTCCCACGCT 720
GGTACCCTCT CAAATTCAAA TGAGGGTAAG AAAAAAAAAA AAAAGACAAA GAAAAGGAAG 780
AGAAACTCTT TTCTGAACAA TCAAATTATA ACCCAATATT GAACCTAAAC TACTAAAAGC 840
TGCAAGCACT TTTCACCTAA TTACATTGTG TGAGAAGAAA CCACTAAAAT TGTTCTCACT 900
CACCATGGAA GTTTTTCCTC TTCTAAAGGT GAATTCTTTC TCCTCCTGCT ACCTGAGGAA 960
GGCCTTGGCT ATTACAGACC ACCCACATGG GGACTTTCTC AGGTGCCTGC CCTGAGACAG 1020
TCATCACACT GTCTCGGCCT CTTCCCTTCT GATTTGGGCA GGACTTACTG ACTCATTCAT 1080
TTATTTACCA TATAGTCGTT TATTCACCAT ATAGTCATTT ATTCATTCAT 1130
|
