| Tag | Content |
|---|
EnhancerAtlas ID | HS020-37443 |
Organism | Homo sapiens |
Tissue/cell | CD34+ |
Coordinate | chr6:7430950-7432410 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr6:7431679-7431693 | AAAATGAGGAAGTG | + | 6.59 | | TCF7L2 | MA0523.1 | chr6:7431269-7431283 | AAAGATCAAAGCCA | + | 6.49 |
|
| | 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 |
| GH06I007431 | chr6 | 7431434 | 7432820 |
|
Enhancer Sequence | AGGAGTTCGA AACCAGCCTA GGTAACATAG AAGACCTCAT CTCTATTAAA ATAAAACTAA 60
AAAAAAATTA GCCAGGCATG GTGGCACGCG ACTATGGTCC CAGCTATTCA GAGGCTATGG 120
TGGGAGGATC ACTTGAGTCT GGGAGGTTGA GGCTGCAGTG AGCCACGACG GTGCTCCAGC 180
CTGGGTGAAT GAGATGCTGT TTCAAAAAAA AAAAAGAAAA GAAAAGAAGA AAAAGAAAAA 240
CAACACAACC CAAACACCAA AAAACAGAAA TAATTTTTAA CTAGTCTTCG TTAAGCAACA 300
TTCTCAATAC TATCAGTAAA AAGATCAAAG CCATTTAGAG GAAGGGAGAA GGTATTATAG 360
CCAAAGCAAA ATAGGCTGCC ATAGCTGGTG CCTCGCTGAA TTTCCTGAGT TGTTGAGCAC 420
AGGGTCAGTG AGCTTGGGGA AGTCATTGGA CATTTCCCAC CTGGCCTGGG TCCGCCCACC 480
TCCACAGTGC AGTGGTTGGA TGCCGCCTCC TGCAGTATTG ACTAACTGGG CGAACGTGGG 540
CAAATCCAAC TTTCTGAACA TACTCCCTTA TCTGAAATGA GGACGGTGTG GAAGGTGAAT 600
GTGCTGCCAG TGAAAGCTCA GAGCTTGACA CCAGGAAGCA CTCAATTAAT GCTGGCTTCC 660
CCTACGAATT CTCAGAGTCT AATACAAATT CACTTGCGGT GTCATTCTGT CGTTCTGTTA 720
CCCTCTTCCA AAATGAGGAA GTGAGTGTTC TTGGACGAAC AGGCTCCTTT GGATTTAAAA 780
TCACCACTCC AGAGCAAAGT GGTCTTTCCA TCCTTAGCAC AGCCCGTGGA GGAGGAAGGA 840
GGATCACTGT GGAAATCGTC CTCACCTCCC ACGCGGCTCC TGGGAATATG TCTCAAGAGC 900
AGATGAGGGC CTTGACCTCA ATGGCAGATC AGTTCACCCT ACATTGTAAA TGGCTCATAT 960
GCGTAGAGCA AACGGTGATG GGTGGAGGGC AGTGGAAGGG GCGTGGTGGG AAGTCCAGAG 1020
AGAAGTCCAG AAAAGAGAGG ATGGAGAAAT CCAAAAGCCA CTGACTTCAC AGTTTTACCT 1080
GGGCCAGCCC TGCCCTGGCC TAAGCCAGGG GGAGGAGCTG GTTGGCTTTC AGGGCCTCCT 1140
CATCGCGTCA GGAAGCCACA CCCCATTTGG GACAAGGGAC CACAGTGCAC AGCTTGTGGG 1200
CTCAGGTGGA GCTGGGATCG GAGCTGCGGC CCTCACCGGG CAGCCTGAGT CCCATAGGGC 1260
GGGACAGCAG GGCGGGGGCT GTGGCACCAG CCGAGCTCCC GACCCTGCGC CACTTGAGAC 1320
CCCAGATTTC CTCTGGCATG TAAGCCAAGT GGTCATTTGG ATTCTGGAGG AGAGCCAGGT 1380
TGTTGTTTTG GGTGCTTATG TTTGTTTTGT TCGTTTGTTT TCGGTTCGTG GCAGCCTCAT 1440
GGAGCATCTA GTTGCTCAGC 1460
|
