| Tag | Content |
|---|
EnhancerAtlas ID | HS082-16515 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr19:4425020-4427130 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:4426477-4426489 | GTTTGTTTGTTT | + | 6.32 | | Nr2f6(var.2) | MA0728.1 | chr19:4426689-4426704 | TGAACTACTGACCTC | - | 6.07 | | Nr2f6(var.2) | MA0728.1 | chr19:4425469-4425484 | TGAACTCCTGACCTC | - | 6.22 | | RARA | MA0729.1 | chr19:4426686-4426704 | TCTTGAACTACTGACCTC | - | 6.1 | | Zfx | MA0146.2 | chr19:4426408-4426422 | CCCGCCTCGGCCTC | + | 6.01 |
|
| | 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 |
| GH19I004425 | chr19 | 4425407 | 4426227 |
|
Enhancer Sequence | CTCGGCCTCT CAAAGCACTT GGATTACAGG TGTGAGTCCC TGCACCTGGC CTGTCCTTTT 60
ATTTGTATGT TGAGACATTT GATGGCAATT GTGTATCCTG AAGGTGCACA ATGTGACATT 120
GTTGTACCTA CACATCATAT TGTGACAGCC AGAGATCCAC ATCATGTATT TTCACTGCCG 180
CATAATACTT CATAATGCAA TGATATGGTT TCTCTCTTTT TTTACAAAAA TTATTTATTT 240
ATTTAGAGAC GGAGTATTGC TCTGTCACCC ATGCTGGAGA GCAGTGGCGC TATCTCTCGG 300
CTCACTCTAA CCTTTGTCTC CCGGGTTCAA GCAATTCTTC TACCTCAGCC TCCCGAGTAG 360
CTGGGATTAC AGGTGCCTGC CACCACTCCC AGCTAATTTT TTGTGTTTTT AGTAGAGACG 420
GGGTTTCACC ATATTGGCCA GGCTGGTCTT GAACTCCTGA CCTCAGATGA TCTGCCCATC 480
TCAGCCTCCC TAATTTTATT TTTAGTAGAG ACTGGGTCTC ACTGTGTTGC CAGGGCTGGT 540
CTCGACCTCC TGGTCTCAAG CATTTCTCTC GCTTTGGCCA CCCACCGTGC TAGGATCACA 600
GGCATGAGCC ACAGAGCCTG CCACTATCTC AACCTCTTTG CCCCTCAGTG GTGTAGGGGG 660
GGTCCCTGCA CATGCTTCTC TGCACACATG CATTCCTCTG GGACAGCCAA GTAAGCATGA 720
GTTCACCTCT AGGACAAAAT AGCATATTGC TGAAGCATCA TGAGCCATGG CCAGAGTGCG 780
TGCCAGATGG GAAACTCAGA TGTACATTCC CGGCGATGTG TGGAAATTTC CTCCCCATTC 840
TCTGCTATCA CTGCAATTTT TATGGGATTA ATTTTCTTTT AACTTTGCCA GTCTGATGGA 900
TTTTTAAAAA TTGACATTGT TTTACTTTCC ATTTTTACTT GACTCTTGGT GCAGTTGAGC 960
ATCTTTTTCT GTTCGTTTGC CATTTTAGTT CTTCTATGAC TTGCCAATTC CTATTTTTTT 1020
ACCTATTTTT CTACAGGATT TTCTTTTTTT TTCTTTGCCT GATCTGTAAG TTTTTTTTAA 1080
CATAGTCTAG TATTTCATTC TCCGTGATAT TTCGTCTCAG CCTGTTACCT CTTTGTTTAC 1140
AGTCTTTTTT TTTTTTTTTT TTGAGACACA GTTTCACTCT GTTGCTGAGG CTGGAGTGCA 1200
GTGGTGCCAT CTCGGCTCAC TGCAAGCTCC ACCTCCTGGG TTCACACCAT TCTCCTGCCT 1260
CAGCCTCCCG AGTAGCTGGG ACTACAAGCG CCCGCCACCA TGCCCCGCTA ATTTTTTGTA 1320
TTTTTAGTAG AGACGGGGTT TGCACCGTGT TGGCCAGGAT GGTCTCGATC TCCTGACCTT 1380
GTGATCCGCC CGCCTCGGCC TCCCAAAGGG CTGGGATTAC AGGTGTGAGC CACCGTGCCC 1440
GGCCTTTGTT GTTTTTTGTT TGTTTGTTTT GAGACAAAGT TTCGCTCATT GCCCAGGCTG 1500
GAGTGCAGTG GCATGATCTC AGCTCACCAC AACCTCTGCC TCCTGCGTTC AAATGATTCT 1560
CTTGCCTCAG CCTCCCGAGT AGCTGAGATT ACAGGCATGT GCTGCCACGC CCAGCTAATT 1620
TTGTATTTTT AGTAGAGACG GGGTTTTTCC ATGTTGGTCA GGCTTGTCTT GAACTACTGA 1680
CCTCAGGTGA TCCGCCTACC TCGGCCTCCC AAAGTGCTGG GATTACAGGT GTGAGCCACC 1740
ACGCCCAGCT ACAGTGTCTT TCATTATACT GAAATTTCTC CTTTTGGCCA GGTGCGGTGG 1800
CTTATGCCTG TAATCTCAGC ATTTGGGGAG GCCAAGGCGG GTGAATCATC TGAGGTCAGG 1860
AGCTTGAGAC CAGCCTGGCC AACAAGGTGT CTCTACTAAA AATACTAAAA ATACAAAAAT 1920
TAGCCGGGCG TGGTGGTAGG CGTCTGTAAT CCCAGCTGCT CATGAGGCTG AGGCAGGAGA 1980
ATCGCCCAAC CCAGGAGGCA GAGGTTGCAG TGAGCCGAGA TTGCACCACT GTACTCCAGG 2040
CTGCGCAATG AAGCGAGACT CCATCTCAGA AAAAAAAAAG AGGAGTTGTG ATCTTTCAAA 2100
AAAAGACCCT 2110
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