| Tag | Content |
|---|
EnhancerAtlas ID | HS108-27165 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:43623500-43625070 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Znf423 | MA0116.1 | chr22:43624969-43624984 | GCCCCCCAGGGTTGA | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 43623697 | 43623884 | | chr22 | 43624336 | 43624849 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I043227 | chr22 | 43623389 | 43623672 |
|
Enhancer Sequence | ATCTGGAAGC ACAGCGGGCG TAAGGGCAGA GGGGAGGCTG GCGGCTGGCG GCTGGCAGGG 60
GAAGGGACCA CCCAGGGCAA GAGGGCAAGA ATCTCCTGAC CCCACCGAGT CGGACAGCAT 120
CACGGGATGC AGATGAGCAG TGCACACGCC ACACGCACAC ACACGCGTGG GTTTATAAGG 180
CTCCTCACAG ACCCCAGCGT CCCTTCCCCC AGGAACCTGG GTGGTTTTCT GAACTCAAGC 240
AGCTGCACCC CAGGCTAGGG GGCAGAGGAG GTAGCACACG ATTAAAGTTC CAACCCAACC 300
AGGTTTTGTG GCGCAGGGAA TGAGCACTGC TCCAGGGATT GTGAAACTGA TTTTACCGTG 360
GGACTCTGGA CAAGCCCTTT TCTAGCCCCG GGTCCCCTGT GGTACAACAG ACACCAGGGT 420
GAAAGAGGTC ACCGCTAAGG CCTTTCCTCC TCTGACCAAA AGCACCCGCT GAAGCTGGGG 480
GAAGGGGCTG GGCCCCACAT TCTGTTAGTT CTTGAGCTGC CTGCACTCGG CAGGCCCAGG 540
GAAGGGGTGC CCAAGTTTTC GAGAGTCTTT CCAGAAGAAT CTGTAGCCCG CCTCCAGAAG 600
CCCAAGCACC AGCTATGTCC TGATCACATT CTTGCCTGAC CCTGTCTGAT CTTCAAGTGG 660
CCTGGCATCG TGAGTGTGGC TACCCCCAGG TCACAGAAAA GGAAGAGAGA GGGGGACCGT 720
CCTTGGCTTC CTAATCTTCA CCCACCATGC CCATATAACA CCAAGTCCCA GCAGCCTGGC 780
TCTGACTCCT AAATACATCT AGAATCTTCC TCTTTGTTCC GTCGCTGCCC ACCCTGCCCC 840
GGCTCCAGCA GTGCATGCTC CCATGCCTGG AGCTGTCTTC CCAGTGGTAC CCTGGATTCC 900
ACTCTCCTTT CCATGTGGTC ACTGGGGCAT CTAGTTCCAT GAACTTGACC ATATCACACC 960
CCTGCTTAAA CCCTCCACAG GCTTCTCATC TGACTGGGAA TAAACCCTCA ACTCCCCTGC 1020
GGGCTCACGC AGCCTGCATG GTGGGATGGC GCCCCCTATC CGCATCTTCC TCTGAGCTCC 1080
CTCCTGTGGG CTCCAGTCCT GTGGCTGCCT CTCGGTCCTT CTGTCCACTG CTTTCTCATG 1140
CGGATCCCTC TGGAGTGCCT CCCTACCCCC AGCCAAACAC TCCCCCTTGA GGATCCCGAA 1200
TTGCCCCTCT ACTCTGCCCC TCTCTGCTGT GAGCCTCCCT GGAACGAGCT GTCTGGAATT 1260
TCCATGTATT GGTGCCCCCG CTCCTGGCCC GAGTTCTCTA GTAAATGGGG TTTCCAGCCC 1320
CGTGCCCATC TGGCCAAGGC CTGGCACTGG CAGAGACCTG CTACCCACCT CTAACCGTTC 1380
CCTGCTACCC CTTGTCTCCC CAGCCCTGCC TCACTTGTCC TTGGCTGAGC CCCTCTGCCC 1440
AGGAGTCCCC ATCCTTGCTG AGGCCTCAGG CCCCCCAGGG TTGAGGGCAG GGTTGGGATG 1500
CGGGGTGCAG TGTAGGTGGC CGTGCGGCCA GGCGCGTGCC TCGGGGGGGA GGTGGCCCTG 1560
GCGGGCAGGC 1570
|
