| Tag | Content |
|---|
EnhancerAtlas ID | HS113-00245 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:10343020-10344470 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr1:10343536-10343547 | TCTTATCTCTT | + | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr1:10344391-10344406 | GAGGTCAGGAGTTCA | + | 6.22 | | Zfx | MA0146.2 | chr1:10343024-10343038 | GAGGCCGAGGCGGG | - | 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 |
| GH01I010283 | chr1 | 10343347 | 10344288 |
|
Enhancer Sequence | TTGGGAGGCC GAGGCGGGGT GGATCACGAG GTCAGGAGAT CAAGACCATC CTGGCTAACA 60
CGGTGAGACC CTGTCTCTAC TAAAAATACA AAAAATTAGC CGGGCGTGGT GGCGGGCACC 120
TGTAGTCCCA GCTACTCCTG AGGCTGAGGC AGGAGAATGG CATGAACCCA GGAGGCGGAG 180
CTTGCAGTGA GCCGAGATCG TGCCACTGCA TTCCAGCCTG GGGGACACAG TGAGACTCCG 240
TCTCAAAAAA AAAAAAAAAA AAAAAAAAAG ATAAAGTTAG AACATTTGAG TAGCTGTTCC 300
AGGTTTATTC AGATAGTTAT TAAATTATAT CTTCTAGAAG TTCACAGAAA GCCTTGATGC 360
CCTATGATTA CTGTACAGGA AGGTTATCTC CTCCTATGCT GGTACCCATG GGGTCACAGG 420
GCCATAGTGC TGCATGTATG CAGATTACTG GCCTATGGCT CCCAGCTTTG CTGTTGGAGG 480
TATTTCCCAG CCCCTTGCTG GCTCTGTCAG GTTCGATCTT ATCTCTTTGT ATGAATATGA 540
AAGTTAAGAG CAGCAGAGCC TTCTGACTCA TAGCTGCTTC TCTTCCTCCT CAATTAATTC 600
AGTGCACAGA CAGTTGTCAC CTGCAGTGCT GAAAGCTGTT CAGGAATCCT GCCACCCATC 660
AGATGACTGT GACAGCATCA TCTGCTTTGA AGCAAATATT TTTTCTTTCC CTACTTGTCA 720
CCTCCAGGAA GATAGTTTGA CCCATACCTT TTAGCCATTG TGTTCAAGAG TGCTAGGGTA 780
GGGGACACAG GGAGGACAAA AAACACTTTT TAAGAGTCTG AGAAGTTGCA GTCATGCTGC 840
CAGCCAGCAG TCTTCTTCAC AGTCACTTGG TATTCCCCTT GACTGCCATT CATGCAAGGA 900
CGATAGAGAA CAGTGACACA TTGACACATT TAATAGGTAA AAGGCTTGCC GAAAAACTCT 960
TTAACACTAA AGTGAATTAA GCTTGATAAT TGAATATGTC AGATGCTTTC ATTTTAATTT 1020
TCATGTGAGG CTGAAAAAGA TTTTATATGA AGAAAGAGGT TCTGCTTTTT CTTTCTTAAT 1080
CAGCCTACCT TTTCCCTTGA CATTTTACTT ACTTCAAAAG TACAGTGTGG GCCGGGCATG 1140
GTGGCTCACA CCTGTAAACC CAGTACTTTG GGAGGCTGAG GCAGGAGGAT CATTTTAGCT 1200
CAGGAGTTTA AGGCTGCAGT GAGCTGTGAT TGTACTGCTG CACTCCAGCC TGAGTGACAG 1260
AGCAAGACTC TATCTCAAAA AAACATGCTT TAGAAACAAA AATAAGGCCG GGCACGGTAG 1320
CTCACACCTG TAATTCCAGC ACTTTGGGAG GCCAAGGTGG GCGGATCATC TGAGGTCAGG 1380
AGTTCAAGAC CCGCTTGGCC AACAGTGAAA CCCCATCTCT ACTAAAAATA CAAAAAAATT 1440
AAGCCGGGCT 1450
|
