| Tag | Content |
|---|
EnhancerAtlas ID | HS050-06043 |
Organism | Homo sapiens |
Tissue/cell | Fetal_stomach |
Coordinate | chr1:225060830-225062310 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYA | MA0060.3 | chr1:225061788-225061799 | TCTGATTGGTT | - | 6.62 | | NFYB | MA0502.1 | chr1:225061789-225061804 | CTGATTGGTTAAGCT | - | 6.09 | | ZNF263 | MA0528.1 | chr1:225061166-225061187 | CCTTTCTCTTCTCCCTCCTTG | - | 6.06 |
|
| | 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 |
| GH01I224873 | chr1 | 225060936 | 225063001 |
|
Enhancer Sequence | TCCAGTATTA CAACCATCAT TTAAAAGTCT TTGAGAAAAG CAGCAACTGT AAAAAATGTT 60
GCAGTGTTGA GCACCCTGGC CAGGCTTCTG CAGTTTGGAG CATTTTCTCC AGCTCTGGGG 120
CTGCAGAGCT GAGGTAGGGT GGCTCCACCT CCTTCTCCAG AGAAGTGACT AGAGCACCTT 180
GAAAGGCTAG GGAAAGGCTA GAGGCTTTAG GGACTCATCC AGCTACTTCT GCCCAGGTCC 240
ACTTGTCACC AGGCTTGATG AGTGTGAGTA ACCCATCACC TTCACGCATT GACCTCCCTG 300
CATCACTCAT TCATTACTCA TTCATTTATT CTCTTTCCTT TCTCTTCTCC CTCCTTGTCT 360
CCTCTCCTAT TCACTCCCTC TCCTTTCACC AACTCTCCCC TCCTCTCCTT CACTGAGGAG 420
GCAGGCAAGA TCAGACACCC AGCTGGGGGC TGGGCATAAA GAAACATGCA TCTGACCTTT 480
TCTACATGAC AACTGTGGAA GTCTGCTGCT AAATCTTTCA TATGATCTGC AATTCTTTTT 540
TCCCACCTAC AGATTACTCC ACGCTTCCTA GCTCTTGTCA TAAATCCACA GATGCCTCAT 600
TTCACAATAA GGAAAACTGA GCCAAGACGG GTTTTAGTGA CTCATTTAAA ATCTCACTGC 660
TGCTTATGGC ACCTCTGATT ATCATCCCCA AATAAAGTTT AAAAGCCACC ACATCATGGG 720
CTATTTTAAA AGATAAACTT AGGCACATTA AAACTTTAAA GAGTATATTT GAGTAGACAG 780
GAATTCATGA ATCAATAACA CTGGACCACC CATGGTTCAG CACTCCACTG TGGGGGACCC 840
GGGAGGCAGA GAGAGGAAAA TTTTATAAGG TGTTTGGGGA AGTAAAAAAT ATTTACTTTT 900
ATATAAAAAA AAATTTGGCT AAAGTGGAAA GTTCCTAGTT AGAGGTTAAC TGGTGGTTTC 960
TGATTGGTTA AGCTTAAGTT TCATTTTTCT GTTTATATTG AGCTTAGGTT TGCTTTTGCA 1020
GGAATCTGAG GCACAAGAGT CTTCTCAGCC TAATGGACTC ACAATTTTTT TTTCTTTTTA 1080
ACAGCTACAG TCCATTTACA GGTTAATCTT TAGGTGAACT CTGGAGCTGA GTTCAAAGTC 1140
TTCCTTGTAA TCCTGGGAAA GAAGAAATGA GAGGCCAGAC CTGGCAATTT CTGAGCCATG 1200
GTCAGAGAGC AAAATATGAG GATCATGTTG ACTGTAGACC TAATGCATTT TTATTTTAAA 1260
ATCCTTTTTC TTAACGAATC CAGACCATTG AAATCTATCT GTAATGGGTT TGCAATTCTA 1320
CTGGATTTCC TACCCTCACT CTTTTAAATA TTGATTTGAT ATTGCCTTTA AAAGTTATAT 1380
TTGGAGCTTG GAGGATTTTA GACTTCTAAT ATAATATTCA GTAAAAATTG AAATATGGAG 1440
GAGATGTGAT GAAATAGCTG GTGACAGCAA CTTCCACAGT 1480
|
