| Tag | Content |
|---|
EnhancerAtlas ID | HS108-26973 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr22:39669710-39671040 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZEB1 | MA0103.3 | chr22:39670406-39670417 | CCCACCTGCCC | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr22 | 39670062 | 39670400 | | chr22 | 39670468 | 39670626 | | chr22 | 39670155 | 39670240 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I039274 | chr22 | 39670321 | 39670470 |
|
Enhancer Sequence | CTAAAAATAC AAAACTAGCC AGGCATGGTG GCGGACACCT GTAGTCCCAG ATACTCAGGA 60
GGCTGAGACA CGAGAATCGC TGGAACCAGG GAAACAGAGG CTGCAGTGAG ACAAGATGGC 120
ACCACTGCAC TCTAGCCTGG ACAACAGAAT TAGACCCTGT CTCAAAAAAA GAAGAAAAAA 180
AAAAGAAATC CTGAAATACA CCTAAACCAA TGGTAACTAG TCTCTGCTTC AGGCCTCCCA 240
AATGCCCCTC GCACTGCCCG GACCCTCCAG AGCCCCCAGG CCTCCTCATG AACCAGTAAC 300
TAGTGGTCAG TGCTTGTGGC AACAGGGGCT CCCCAGGCCA CCCGATTGGT CAGCACCAGC 360
CCTGCTGGGT GGAAAATGCT CTCCCCTGTT CTGGCCCACA GTAGGCACTC AGTGGGCATA 420
GCGGGCTGGA AAAGTGATGA CTCAGCCTCA CTCTTTGCTC CCCACCGCAG ACCCCATGAG 480
GGAATGGCAC CTCAGCACTA CAGGCTGTGC CCCCCTTCCT CTGGGGCCAG TGGATGTGAG 540
GGGACTGTAG GGTGCAGAAC AAGAGGGCTT TGAGGCAGCC CTATCTCCGG AGGGAAGTGG 600
AGGAGATAGC ACAGCTTCTC ACTTTCCCAG CCTGTCCCAG AGCAGAGATA ACCTGGAGGA 660
GACGGGGTGC CTGGAGCCCT GTGAGCAATA GGGCCACCCA CCTGCCCCCC AGGTCTCCCA 720
CAGTCCCTGC TATCGCAGAC TCCAGGCTGA AACCCGAGGA ACCGCTCGGA AGAGTGGCCC 780
AAGACAGGCA GGTGATAAGC TGGGCCAGTC AGCATCCCCT GGAAAAAGGC CTGCAGGCTG 840
CAACTGCCCC TTCCGCAAGC CTGGTGCCAC CCGAACCTGC CCCGGGGAGC CCACCATCAC 900
CTGCCCCATG CTCCCCAGAG CTGCCCTAAG ACATGGCCTC AGCCTAGCTG CCTTCAAAAG 960
CGCCCGGTCC AGCCCTCTTG CTGACCAATG AAGAAGCTGA AAACAGAGAG GCTGGGGGTC 1020
TTGCCCAAGT CACACAGCAT TTTGATGGCT GAGGGAGGAC TTGAACCCAC ATCTCCTGGC 1080
TGCTGCAGGG AACACACCAG ACTGCTGTTC TCAAATACGG CTCAAATATT AAGAGAAGGG 1140
GGCAGGGGGC TGGAAAGCAC TAGGTCTAAA CTCCAGAGGG GTGGGTTGGG GAGTGCAGAG 1200
AAAGAGGCAG AATCATGTGG AGAGTCTGGA GCTGGGAACC AGACAGCAGG TTTCTGTCTC 1260
CAGCTCTGCA ACTAACCCAC CGTGACACCT TGACCCAGTC TCTGCTCCTC TCTGAGCCTC 1320
AGTTTCCCAA 1330
|
