| Tag | Content |
|---|
EnhancerAtlas ID | HS062-12104 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr4:15458380-15459790 |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr4:15459373-15459392 | TACTGACCTCTAGTGGCCA | - | 7.12 | | RUNX1 | MA0002.2 | chr4:15459695-15459706 | CTCTGTGGTTT | + | 6.14 |
|
| | 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 |
| GH04I015456 | chr4 | 15458552 | 15459623 |
|
Enhancer Sequence | CAACATCACA AGCAAGCCTG CAGTCATTAG AATTGTGAGG GGACTATATT AATCCACCTC 60
CACTGATAGG ATTTGAGAAG GGCTTCCATT TAATCCCACT CCTCACCCCT GAGGGTGCCA 120
AGCCAATTGA GAAATGCACA CAGAAGCCAC ATATGTACCA AAATACTTGT CTTCCTACTG 180
GTAGCACCAA ATCAGAGAGA GCAACTTGGA TATGAGGTTG AAACAAACTT CCCAGTAGTT 240
GCCTCCAGGT CTAGACCTGA TTAGCATCCC ACAACAGAAA CTTTTCCATT CAGCCTCAAA 300
GAGAACAGAG GTCTCCCTCC CCTCAAATCA AGCTCATAGA ACCCAAGAGA GGCCACATGT 360
GCAAGTGACT TTTTACACAC AGCCCACTCC CAACACAGAG CCCAGGGGGT ACCAGACTCT 420
TGCCATCTCA CCAATCAGAG AAATCCCTCC TCCTCCCTCC ACCAGAAGGA GCCATGGAGA 480
GGTAAGCCAC TAATTATTAA GAGAGTGGAA GTTCCTATCT TTCAGAGCAG CAGGAACTCA 540
GGGAAAGGAA CAAAAATTGT GCCTTCCCTA CCACATCTAT GAGAAAAGAG CTGATCTAAA 600
AACATATTTA CCTTTTAATT CTCAGTGACC AGATAGGGGC AAGTGCACCA CTGGATACAG 660
TGAGGGGCTT GCTCTACAGA AGAGTCATTT TCAGTTCCTC TTTCCTCCTG TTACACAGCT 720
ATCAATGCAT TCAGGTCTGT GCAGAAACCA TACGTTCTTC ACTAGCTAGG GCCAGACCTT 780
CTGCTCCTTC ATCTCTCACA CTAAGATTGT TAGTGAACTC TGCAGTGAAT GCTCAGCCAG 840
AGTTTGGAAA TGTCATCTTA CAAGCTCTAA TATGTCAAGG AGAAAACTGT TTCTTTGGGA 900
ATGTTTCTTC CTAACCAAGA TAAGAAAACA GTAATTTTGC TTTTGCTTCA AGGCATACTT 960
TGATGGCAGG AGAATCCAGT TTACTTTTTA AGGTACTGAC CTCTAGTGGC CAGCAACAAT 1020
AACTACTCTA TTAGAGACCA TTTCCAGAGA TTATGTAAAA TCCAAGTGCG GGCTAGGAGA 1080
AACTTTAGAA ATCAACTTTC TCTGCCCACC TCATATTCCA GAAGAGGAAA CAGAGATCCA 1140
TAAACGATGA GGGCCTTGTC AGTGGTCGCT AAGATGGGAC TAGAGTCAAG GTCTTCTGTC 1200
TTCCATGTGG ATCTCCTCCC ATTGCCTAGT ATACATTTAT TAAAGCTACT TAGTCATATA 1260
CACTGTAATT CATAAACAAT TAGAGTAAAA ATGACATTTC GTTATCAGAT AATCCCTCTG 1320
TGGTTTCCTG CAAAGCTTGA TGGGATAAGT GTGACTAGAG GTCCGTTTTC ACGCTGCTGA 1380
TAAAGACATA CCCAAGACTA GGTAATTTAT 1410
|
