| Tag | Content |
|---|
EnhancerAtlas ID | HS010-03339 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr4:57623360-57624900 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SCRT2 | MA0744.1 | chr4:57624777-57624790 | ACGCAACAGGTGA | + | 6.22 |
|
| | 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 |
| GH04I056757 | chr4 | 57622837 | 57625432 |
|
Enhancer Sequence | ACAGCTTTGT ACATGAAAAA ACTAATACAC AAAGCCCGTG GTTGGCTTGA AGGAGGTAAG 60
GAAGAGACTC TCTGTATCCT CTGGTTGTGA CTGTTCAACC CATCCCAAGG GATGTAACTC 120
CCAGTGCAGT GTGCTCTGAC TCACAGGGAA CAGCCAGCTT AGTGCCTGTC AAGGCCTTCC 180
CTCCCAAACC CCAGGCAGCT GGATTCTGCA GGCTGGTTCT GGATCTGGGT GGTACTTTCC 240
AGGCCCAGCC TGACACCAGT TTTAAAGGCC ACCCCGGGTA TCTATGGGCT CTGGGAGACG 300
TAGGATGGAA ATGACCCAAG GCCTGGGATA TACACCAGGC CACAGCCAGA ATGCAGGCAG 360
TTCAGGCAGC ATGTGTAGTA AATACACACT AAGATGTAAT CCAGCAGGCC CCCCTGTACC 420
ACGCCCCACA GGTGGCACCA GCGTATAAAA CAACCTGACA GCTACGGGCT GGAGAAGAGA 480
CACAGGCTGG CCTGGACAGG GTGTAGACAT TGTTAAACAC TTAGTTGAGT ATCTGTGGGC 540
AAGTCTTGAG ATCGCTAAGT AGAATCTGAG CTTTGTTTCT TTGGTTTTTG GTCTTTTTTT 600
TTTTTAAAGA AAGTACAAAT ACAAATTATG TGATTCCCTT TTCTCCTCTT AGACTGCCTT 660
GCTCATCTGC TGCTTGGTCG AAGCCATTTG CTCCTCCCCC ACACGCTTTG CTCATCAAGC 720
AACCAGAGCG TTCCTGCCAC CTGAGTCATT CTGTCCTGTG CTGCTCTGTC ACCCTGTGAG 780
TGTGAAGCCC CTGCTCCGGC CCTCCAGGAG GAAGGAGGCA GAGTGAAGCC AGGCATCTCT 840
GGAGCCATGC GTTTGGCTTC AAAGTAGGAG GGACTGGGAC TCTTAGGATG GAAAGTCTAG 900
GGTAGGAGGG CAGGAGCTTG ACTTTCAGCA ATAAGGTAGG GAGGGAGGTG GTTTTACTGC 960
AGAGGACTGG GTTTTACTTG CTATGAGCCT GTTTAGCTCT TTAAGAGCTG AACCTAAGTG 1020
TTTTTTTTTA AATATAGTTA TTTATTTTGG GCTCCAGCTT CCTGCAGTTG CGGTTTCTGT 1080
CAGACTAGTT TGTTAAAAAA AGCACTTAGA ACACATACCA GAGGACAGGA AGAAAGCAAA 1140
ATACTGGCAC TTTTGAAAAG TGTTGTTTTT ACATGACTTG AATTTTAGTT CCTACTCAGG 1200
GTTAAAGGAA GTTCTCTTCC GAATAAAGAG TGCCTGTTGG GTGAGAGAGG ATTTGCAACT 1260
GGAGTTGGAG ATTCTGTGTC ATTGGAGACA TTTGTTCGTA TGCATGGGCT TTAAAACACC 1320
AAGAAAAAAT ATACAGGAGA GTCCTTCCTT TTGTTATATA CTAGCTGTGT TCCTGAAAAC 1380
GTATATGAAA ACATTAAAAA ACTGATCCCT ATTCAGAACG CAACAGGTGA GCTCACTAAA 1440
GGGCTCTTAC CAGAAAGTCT TATAAATTGA GGCACTTGAA GGGCTGGGAC TAGGGTGAGG 1500
TAAGGAAGGG GATGCCTAGA CTCTCGGTAA TTAGGATAAA 1540
|
