| Tag | Content |
|---|
EnhancerAtlas ID | HS060-14889 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr17:43456590-43458090 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Gata4 | MA0482.1 | chr17:43456773-43456784 | GGGAGATAAGA | - | 6.62 | | Nr2f6(var.2) | MA0728.1 | chr17:43457247-43457262 | GAGGTCAGGAGTTCA | + | 6.22 | | ZNF263 | MA0528.1 | chr17:43457129-43457150 | CCCCTTTCTTCCCCCTGCACC | - | 6.01 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCTCATGCAG CTCACATTCT AGTGGGACAG AGCAAACTCA CCAGAAATCA AAACGTCAAC 60
CTCCTCCAGG AAGCCTTCCC TACCCTTGTC CCCAAATCTC TGGTCTCCCT CAGGCCCTAT 120
GCCCCTCCCC CACGACACGC ACCATCCTGT ACTGTGAATT TCTCTCTGTA TCTGACTCCG 180
CGTGGGAGAT AAGAAGACAG GGTTCTTGCC GTTTCCATCT TATTCTGACC AGCACAAGGC 240
CAGCACTTGG TGGTAACTGT ACCTGTGGGT TGACTTCCAC CGGTGGAAAA GGTGGGGCTG 300
AGGGACGGGC ATGGCCACAG CCAGGGGCTG TGTAAGTGCC TGCATATTTG GGGAGAGCAA 360
GGAGTGCAGG GGAGCGGGGT GAAGTGAGAT GCTCATTGTC TCGCCAGATC TTGGAGGGCA 420
GCACAGGTTT CAAAGGGGTT CTATGGCAAT TTTCTTGTTA AAGGAATATG GCCCAATTTA 480
TCAAACCACA AAGGGAACTG TGAACTCAGT CACACGCAAA GTCATATCAA AACAAGGTGC 540
CCCTTTCTTC CCCCTGCACC TGCTGATTAC TTATAAAAGT TTAAAATAAA GCGCCGAGTG 600
TGGTGGCTCA AGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCGGGCGA ATCACTTGAG 660
GTCAGGAGTT CAAGACCAGC CTGGCCAATA TGATGAAACC CCATCTCTAC TAAAAATACA 720
AAAATTGCTG GGTGTGGTGG TGCACACCTG TGGTCCCAAC TGTTCGGGAG GCTGAGGCAG 780
GAGAATGGCT TGAACCTGGA AACTGGAGGT TTCAGTGAGC CGAGATGGCA CAACTACACT 840
CCAGCCATGG TGACAGAACA AGACTCCATC TCAAAAAAAA TAAAAGCATC CCTTTCTTAT 900
GCAGCAAGTG CCTGGCTTAG GGAACCTGTT ACCCTTCTGC AATGAAGTAG AAGTTGGAGG 960
TGCTCTTATG GGTGACCTAT CCATATAGGG TGCTAAAGGG AACTGGAATG ACTTGGGGAC 1020
ATCCCTAACC TTTGAGGCTG ACGTCATGGT GATAACCACT CACCCACAAC ACATCTTGTG 1080
GTGCCAGTTC TCCATAAGAT GGATAAGGTC CCTAAACACA CGGCTGCACG TCTGATGTTC 1140
TTATGAGCAC GCAAAAGGAA CCAGGCCCTC CCTGCCAGGA AGCTGCAGGG AAATTAGAAT 1200
CATTTGACGA GTTGTCCATT CTTTCATTTG TCTAGTAAGG AGGTACTGAA AGCCTCCTCC 1260
TAGGAGCCGA GTATGGTGCC AACAGCTACA GGAATGGCAA ACCATATAAA TAGCCCAAAC 1320
AGGATATAAT TAGCGTCGGA CGTGCACATG TCATGGGTGG AATGATGCAG AAAGAGTGAT 1380
GCAGCCCCCA TCTGGGGCTG GCATCACATG GGACGAGGCG CTTGAGCTAG ACATGGAAGG 1440
ATGAGCAGTG TGATCGCCAG GTGGAAAGGC ATTACAGAGG AACGGCATGT GCAAACACCT 1500
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