| Tag | Content |
|---|
EnhancerAtlas ID | HS108-01435 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:40294200-40296560 |
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 | chr1:40296271-40296283 | GTTTGTTTGTTT | + | 6.32 | | Foxd3 | MA0041.1 | chr1:40296275-40296287 | GTTTGTTTGTTT | + | 6.32 | | ZNF263 | MA0528.1 | chr1:40296006-40296027 | CCCTTCCCTTCCTTCACCTCC | - | 6.16 |
|
| | 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 |
| GH01I039829 | chr1 | 40295095 | 40296543 |
|
Enhancer Sequence | TTTTCCATTT TTCATAGGAC TTCATACTGA AATTTTCTTT ATTGCTTGTT ACTTGCATTA 60
TTTTCTTTCT CCCTATGAGA ATGTAAGCTG CATTTGGGCA GAAACCCTGT CTGTATTTTC 120
CCAGCAGCAG AGCTAAGCCT GGCACTTAGT AGACACCAAA AAAACACTTG AATGAATGAC 180
TGAACAATTT AATTTCAATG TTATACTGAG GCAGCACAGC GCAGCACTTC AGAGCAACGA 240
CTTTGGGGCC AGACCACCTG AGTTCACCAG CTCCCCATCT CCTGCCTGCA TAAACTTGCA 300
CACATTGTCT TACTAATCTG TGTTTCAGTT TTGCCATATG GAAAATGGGG TGGAGGGGGA 360
GGATAGCAGT ACCCATCCTT CAGTATTGTT ATGAGGATTA AATGAGTTCA CACATGTAAA 420
GGGTTTGAAA GGGCTTGCCA CAGAGCAAGC ACTCAACATG TCCTCACTCT TATTATTCAC 480
TATTAATCAT GAGTCCACTC AGTTGAATTA TCAAAATTCA TCTTTCATTG TTCTGCCCTC 540
CATAGCTCCT CTTTTATCTT ATTTTCATGT CTTTTATCAG TTTCCTGTGT TCTGGGAGAC 600
CATCTGAAGT TTGTTTTCTT TACTAAATTG ATCTTCTGTG TTGGACCTGG CATTCGTTGC 660
TTCCATGCAG TTTTAATTCA GCAGCCATGT CTTTAATCTT CTCCTAATCT CTTCTTATCC 720
CAGATTATTC CAGTTGTAGG ATTGCTGGTT CTAAGTGAAT TATGTACCAT CTTTTGAATC 780
CTACTGAAAC TTCAATCAGG TATCACCTAC ATTTTCTTCT ATTATTTGCA ACAGGTCTAT 840
TTTCAGAGGT AGGTACTCCT CTAAATCTTC AGAGAAAAGC TAAATCACAG TCTCTGCAAC 900
TGCAGACTGT GCCTTACCTA ATCCTTCTGG AAGGAGGTCT CTACAAAGGG TGACTGATCA 960
TCTTGGTTTG CCCCCACTGA GGGGTTTCTC AGGACATGAG ACTTTCAGTG CTAAGACTAG 1020
TAAATCCCAA GCCAAACAGG ATGACTTGGT AACCCCACCT GTAGACAGTG TCAAGGAAGA 1080
GCTGTATTAT ATTAAGAAAA ATGGTCTTCC AAATCTTTCA CAAAAGGAGG AAACCATTTT 1140
CTAGTATTTA GAATGACTAG CTCCTTCCAA TTAGCATTTT AAAATGTGAA AGTCTCTTAG 1200
AAAGGGGGAA AAAAAAAAAC CTGCTTCAAC CCCAAGCCTC CCTTTAGCAA CCCCCTCTCC 1260
TTCCTTTCCT AACTTAGACA CTCACCACTT TCTCTCCTCC CATTCACTCC TCAAACCACT 1320
GGAATATGGC TTCCATTTTC TAACCCTCAG CTGACCCCTC TTTTACCAAG GTTACCACTG 1380
ATGTCATCAC TAAGAACCAA TGGATACTTC TCATTCCTTA TTGTGCATGG CCCCTACACA 1440
CTTCCCTGCA GACCACTCCC TTCTCAAAGC TCTGTAAAAT GCTCTGTTAA TGTTCAAGGC 1500
TCTGCTCTAG ATTGTTTCTC TTCTCACTAC ACCCCCTGCT CGAGTGACCT CATCTTCCAC 1560
GGCTTCAAAT ACCGTCAATA CTGATGACTC TGAGATCCCT ATCTCCAGCC CAGAGTGCAA 1620
TCTGGGCTCA ACTCGAATAT CCAGTTCCAT GAGGATTCTC TACAGATGCC TCAAACTCCC 1680
CAAGTCTCAA ACTGAACTCA TCCTCAACCC AAACCTGCTC CTCCTCCAGT GTTCTTATCT 1740
TGGCCAAAGG ACTTGGCCAC TGTCTAATCA ACTGTTCAAG TCAGAAACCT CAGCCTCATT 1800
CCTGACCCCT TCCCTTCCTT CACCTCCAAC ATTTCATCAA GTCCTATAAA TGCTACCTGC 1860
TAAATATCTA AACTGTCCCC TGCCTCTAGG CTGTCTGCAG CCAATCCATT CTCTGCATTG 1920
CACCAGAGTG ATCTCTCCAG GAAACACGTC TGATGTTTTC TCGGGATTCA TGGTTTACAG 1980
GGTCCTCTAT GACCTGGGTC CTGCAGACCC CTCCTGCCTT TTCCCCGAAC ACTCTCCTAC 2040
CTGGCTCCTG CCCATTATTC TCAGGTTTTT TGTTTGTTTG TTTGTTTGAG ATGGAGTCTC 2100
ACTCTGTTGC CCAAGCTGGA GTGCAGTGGC TGATTTTGGC TCACTGCAAC CTCTGCCTCC 2160
TGGGCTCAAG CAATCCCCCT GCCTCAGCCT CGTGAGTTGC TGGGACTACA GGCACATGCC 2220
ACCATGCCTG GTCTCGAACT CCTGACCTCA AACGATCCCC TCACCTCAGC CTCCCAAAGT 2280
GCTGGGATTA CAGGCGTGAG CCTTGGTGCC AGGCCTCATG TTTTTTCAGA TGCCATTTCC 2340
TCAGGAAAGC CTTCCCAGAC 2360
|
