| Tag | Content |
|---|
EnhancerAtlas ID | HS050-65755 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr8:40228460-40229890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr8:40228882-40228903 | TTTTTCTTTTTCTTTTTTTTT | + | 6.09 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 4 | ID | Chromosome | Start | End |
| GH08I040369 | chr8 | 40227461 | 40228844 | | GH08I040374 | chr8 | 40228861 | 40229010 | | GH08I040371 | chr8 | 40229181 | 40229330 | | GH08I040372 | chr8 | 40229822 | 40230168 |
|
Enhancer Sequence | GAATCTGAAA ACACTTAAGA AAGAGGTTTG TGTGGAGAGC AATTATTGCA GTTTTTCCTA 60
AAGCTATTGG AGCGGAGAAC TTAATTTAGT TACTTTCCAG CAGTCTTTAT CTTGTCAGGC 120
TCGTTCTTTT CTGCAGACTT TCAGGGAGAC TTCTCAGGAG CCAGGTCTGT ATCTATCCTC 180
ATCCTGTCTT AGCATTTGCT GAGATGCAGC TCGTCACTTC TAAATCACAT CTGATCTTTG 240
GTTATCTTGT TTAGACTACT AGCACCTCCC TGGATTCTGT AATTCACTTA AAATCACATC 300
AGCCAGAACA GTGTGATCTT ATTTGTGTGT TATTTAACAC TCTATCGTAG GGCAGTCAGT 360
CGCCTTATTC TGGAATTCCC ACTGTTAGCA TTGCAGGCTG GCCTACTCTA GAGGTAGCTC 420
CTTTTTTCTT TTTCTTTTTT TTTTAATTTA AGCTGAACAA ACACGTAGTG TTTACTTTAT 480
GACAGGCACT GGGCTAAATG CTTTATAAAT ATGAAGTCAT ATTAGTACGT GAATAATATA 540
AGTGCTTTAG CTATCTTTAT CTCCTGCCAA CATCAGAGGC TTTAGGAATT AGCATGATGA 600
ATATTAAATA TGGGTTCTCA TAGTTGAGAT TAGTGGTATT CAAACTGCAT GTCATGACTA 660
GAATATTGCA GAGGGTCTTC TCACTTTTGC ATGAACATCT AATCAGCTTT GCAACTTTCC 720
TGTAAGGGAT AACACTTGGA GTTTGATTTC TAAATGGCCA GATATTGCAC AGTATAGTGT 780
CCAGCTATTA GTCAGAAGAC ACTGTTATGT AATACTTATT CTCATGATAA AAGAATTCTG 840
TCTTTAGAAT ATTGTTTTCT ATCTGCATTA AATGAGAATT TTACACAGGA TTGGTTGAAT 900
GACCTAGATA TAACGATTGT TTTATGCCTA TTAGCTAACA AATGTTTATT TAGTAAATGT 960
CCAAACATGG GAAAGATTTC AGTCTGAGAC TTGTTTTCAT TATAATCTTG TAGCAAGACT 1020
GCAGAGCTAT AGCTACTCCT CACCCAACTC AAACATTTTG GTGACTACTG TTATCTACCA 1080
GAAAGAACCT GTGAGTTGTA TATGACCAAA TCAGCCAGTT TGCAACTTCA CAATAGCAGC 1140
TCTGTTTCCA GCCTCCAGCA AGAGCGGTCC CCACACCATC TGTGGCTATA ATCTCTCACC 1200
AAGACTGTCA GATTGTCGGG GGCCTCTGCT TCTCAGGTTT ATAACACTGC TGCCTTAGAC 1260
ATGTGGTAAA TGATTTCACT GTTCCCTGTG GGCATGTGGG GTCTTCTTTG CAGAACTTTT 1320
CTCTGATTCC TCCTAGCTAT AGCAGAAGGA GGAGAGCTGC AATGCTTGCT GATTTCTTGG 1380
GATCTGGACG AAACCATCAT TTCTCCCCCA GTGGCATCTC CCCTGTTGTG 1430
|
