| Tag | Content |
|---|
EnhancerAtlas ID | HS134-01847 |
Organism | Homo sapiens |
Tissue/cell | Mesendoderm |
Coordinate | chr1:67798430-67799870 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TBX21 | MA0690.1 | chr1:67798980-67798990 | AAGGTGTGAA | + | 6.02 | | TBX2 | MA0688.1 | chr1:67798980-67798991 | AAGGTGTGAAT | + | 6.02 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 67798444 | 67799772 | | chr1 | 67798461 | 67799300 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I067332 | chr1 | 67797898 | 67799828 |
|
Enhancer Sequence | CAAGTTCAAG GTAGTAAGTA GTCTGAAAAA TATTTAAGTT ATATCACATT AAGCTAAACT 60
ATAAACTAGG GAAACTCTGG GCTTGTGAAT TCTTGTCATT CTTACTCACA TATGATAATG 120
ACCTAGTTAG AGATGTGTGA AAAGGTTTTT CTTTTCTTTT TTAAAAAGTG TTTGTCTTTT 180
GAATTAAAAT TCCTTCAAGG CAGCACAGTA ACTTTCTTAT TTCCTATAAA ATAAACCACC 240
ATCATAACAA TGAGTATAGC AACTCATTAT GGTTATGAAC TCATGGATGA TTATGAATTG 300
AACCTAGGAA GCTGGCTTAT TCAGTCACTG AAGGTATTCA TAAAGAGAGA AACCCATACT 360
CTGAGATACA CCACCTTTAC CAAGCTCTGT TGGCTTCCTT TCTGTCTCTG AATCTCCCTT 420
TTCTATGTTT GATTTTTCTG TGGGTTGTTG TAGGTCTTTT TTCTCTTACT CTAGGCTGCT 480
TGGTTTTCAC CCCTTACCCG CTGTTTCTGT CATCAGTTTC TTTATGAAAC ACCAACTGAT 540
GTAAACGTAA AAGGTGTGAA TTTTTTTTAA CACGTCTTCC TTTTAACCCT TTCAATGTGT 600
ACTCATATGT AACTTGGCAT TTAAAAAAAA TTAATAGTAA GCTTTTTTTT TTTTTTTTTT 660
AGGTACTCTC TAAAACTGTG AATGACTCTA CAACAGAGTC AGCCTTTTTG CAGCCTTTGC 720
TTCTCAAAAT TGAGAGAAAT GTAACATCTC CGGGTGGATT GGTGTAGTTG TTTATATCAT 780
TTGAACAGTG GGTTAGGGCT TCCTTTACTC CATAGGGCCC TTTACTATGT CATTAAATTC 840
AGCTCCTATC ACTGAAAAAC ACTTTTTAAA TGACCGAAAA GTAAGGGATA GGAGGAAAGA 900
AACTACTTTG CTGTGTTTAA GAGAACAGTC TTGAAATCAG CATCCATCAA AGGCAGGCCT 960
GATAGTGACA CTGGGAAGAG AGCAGCCACA TTTTCCTTGT AGTGGGAAAA CATTCTTGAA 1020
TTTGAGCTCA AGGTGTCCAG ACATGCCTGA GAACATGCAC AGGTATTGAG GGAAGGTGAT 1080
CTCTCACCAC TTAGAACACC CAGGAAGAGA TGCCAAAATA CTGATTAATC AGCTATTCCT 1140
TAGAGCTATG TTACCAATAT GTCTCTGTCT GTTAATCCGC CATTTTAAAA AGTCTTATTT 1200
GCAGTTTGTG ATCTTGCTCA ACTCTATTAC AGCTAACAAA GGAATCGTTG CATGTTCATT 1260
CGTACTTTGG AGGGGCAGAG TGGTAAAGGA GAAACCTTCC CCCATCATGG TGACAGCAAG 1320
GGTGAGGGGT GAATAATCCC TAAAGGGGGA GAAAATGAAG AGTTACCAGC TGCAGCCACC 1380
TCTTCCCACA TTGAGAAGCT AGGAAATTCA TGCACTCATT TGTAATTTAA AAATATTGCC 1440
|
