| Tag | Content |
|---|
EnhancerAtlas ID | HS020-33166 | Organism | Homo sapiens | Tissue/cell | CD34+ | Coordinate | chr4:3413370-3415790 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REL | MA0101.1 | chr4:3414968-3414978 | GGGGATTTCC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr4 | 3415154 | 3415446 | | chr4 | 3413559 | 3413746 | | chr4 | 3415027 | 3415356 |
| Enhancer Sequence | TTAGGCAAGC ACAAAGAGTC AGCCCACTCC AAGGACCCCT GCCCCAGAGA GAGTGAGTGT 60
GCAAGTTGAG TGTGTGTGAG AGTTTCACAC CTGGCTTACA TGCAGAACGG GGCACTTGCC 120
ACATGGGGGG GAGTCTTGGA TGTTGGGATT CTTTGAGGGA GCCTCACATG GCCCCTGTCC 180
TTCTGTCCTT GGCCCCAGCC CTCCTGGCTT GGCCGCCCTG TCCTGCGTGT GAGCGCTGGT 240
GCGCGTCTTC TTGCAGTGCG TGCCGCCCCT TCCACCGCAG CTCGGAGTCA GGGCTTCCGT 300
GTGAGCCCCA GCCGCAGGCC TCTGAAACTT CAGTGCGTGC TGGCGGCCAC CGCGGTCACA 360
CATTTGATCT ATAACAGATC AACAGCATGG TGGATTCAAG GAAACATTAC CACCGTGTTT 420
CTGATCCTAT CCCAGAACTT CCTTTCGGTC TTCTTTTAAT TTTTTTCTAT AGCAGTTTAC 480
ATTATTTGAT TATTCTTTAA CATTTTCTTT TTTAATCTAA ATGCTCTTCG CACTTTGAAT 540
GACTCCTGCC GAGCGTAGCC TCTGGCTGCC ATGCTGACCA TGAGGGACAC TGTTGGATCA 600
AAGCCCTGGT TTGGTCTCCT GGGCTCTAGG GCTCCACTTT TCTCTGGATT AGCGGGGCCC 660
ACGCTGTGGC CTCCTTGGAA GCCTCCTGCC AGGCCTCTGC CTGTCGCCTA CAGCACGTCT 720
GCAGACTGGG CTGAATCCAT AAGGTTTAGT GTCGCTTCTG CCCCTGAGAG GAGTTGATGC 780
TGCCTCACTG ACCCCCTCCT GGTCTCTTTC TACCCCTGGC CCCTTGCTGA TAATAAGATG 840
TGTTCTATTT GCTGGCCTGG AGCTGGAGCC CATCAGCTCG TCCGCTGGGA TCAGTCCTGT 900
GGCCTTGACT TTACAGCAGT GCCAGCCTGG GCGGCTTATC CTGCGCACCG TGCCACAGGA 960
GGCTGGTGAA GGGGCAGGAG GGGAACATAG CGTATTTTAT TATGCTGCTG AGAACATTCT 1020
GTGAGGCTGC TCTGTCAGTC AGCTGCATTC CATAAAGCTG CAGCAGAAAA CCAAGCCCAA 1080
AGCCCAGGGC TTCTTAACAA CACAGGTTTA GTGGCCACCT TGTCACACGT CATCTGTGGT 1140
CAGCAGGGCA TGGCTCAGCT GCAGGCTAAG GACAGCCCGT GTGGGACACC CTATGCTCAC 1200
AGAGGAGACA TACGTGCTCT GGCACGGTGG GCAGCGGTCC CTGAAGCTGG GCTCACACTG 1260
GCCCACATCC CTTCTTGGGC TCAGGCCAGG CCGGCCACTC TGGGACAGGG GCGCCCCCAC 1320
ACTGCTCACG TCAGGAGGGA CGGGGGCGCC CCCACACTGC TCGCGTCAGG AGGGACGGGG 1380
GCGCCCCCAC ACTGCTCGCG TCAGGAGGGA CGGGGGCGCC CCCACACTGC TCACGTCAGG 1440
AGGGACGGGG GCGCCCCCAC ACTGCTCGCG TCAGGAGGGA CGGGGGCGCC CCCACACTGC 1500
TCGCGTCAGG AGGGACGGGG GCGCCCCCAC ACTGCTCGCG TCAGGAGGGA CGGGGGCGCC 1560
CCCACACTGC TCGCATCCAG TGGACAAGGG TGATGAACGG GGATTTCCTG GGGACCTCCC 1620
TTCTCTTTAT TCGAGAGCTC AGGAGATACT GGGAACCAAA GGCTACTGAG GGCCGTTTTG 1680
CAGACACGTC AGGCAGGATC CGGTGTCCTG GGAGCGCGCT GTGCCATATC CCACATCGGG 1740
TCTCCTGTAA ATGAGCCGCC GAGCCGACAT GCGTGGCTGA GGGCTTAGCT CTGGACACTG 1800
TGCCTGAGAG TTTCGTGTTG AGAAGGAGCC CACATGCAGA GCAGTGTGCA GTCACGGGTG 1860
TGTGGGCTTC GCATCCGGAA GGTGAGCCTC GTGCCCCCTT CGACTGAGCA CGCTCCCGAG 1920
GGCACCGTGG GTCAGGACGT AACTCACGTG GCATACGCGG CGCCCCGCGC CCAGCTGCTT 1980
TCGCTCTAGC AAGCCTGTTT GGGAAACATC TTGTTGCCAT GATGGTCTTA GTGCTCTGTG 2040
TGCACATGCT CCTGTGTAAG GTTAGTTGCT TTTCCTGTTC AACCCTGTGG CTGTAGTTTG 2100
TTGTTGCTTG GGCGAGTGTG CACGTGTGAG CATATGAGTG TGCGTGCAAG GGTGCTGTGT 2160
GGGCCTGCAC ATGTGAACAT GTGTGTGTGC TCGTGCACAC ACATGTGCAG CCGCTCAAGG 2220
TTGGGGTCTG TGTTTTGTTC CCTGCTCCAT CCCTGTGTGT AGAATGCACT GGCAGGTGGT 2280
AGGTGTGCTG TGCATAGTTG TTGACTGAAT GGGTGTTGGA GGGGACAGAG CTTGCTGCGT 2340
GTCCCAGGGT CTCCTGTGGG CGGGCAGAGC AGTCACTGGG CCGGGGCGGA GGGCAGGGGT 2400
GCAGGTGCTG TCTGTGCTGG 2420
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