Tag | Content |
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EnhancerAtlas ID | HS073-08236 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr2:60640260-60641320 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RREB1 | MA0073.1 | chr2:60641035-60641055 | CCCCAAAACACAAGCCCTCC | + | 6.16 | ZNF263 | MA0528.1 | chr2:60641271-60641292 | CCCTGCCCTTCCCCCTCCTCC | - | 6.1 | ZNF263 | MA0528.1 | chr2:60641274-60641295 | TGCCCTTCCCCCTCCTCCTTT | - | 6.83 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I060412 | chr2 | 60639852 | 60641878 |
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Enhancer Sequence | ATTCCCCTTC TGAGAAGGGG TAGGAGGTGG GGTGCTTGTC CGTCACAGGT ACACATTGTG 60 TTTCCATCTA CATGCACCAT GCCATGCCCC CACTGCTTGT AGACAAAAAG GAATGAGTCA 120 AATAACTGTC AAGTGACTCA ACACTTGACA GGCTGTGTGG CCATTATGTG GGTCCCTTCC 180 ATACTGGCTC CTGGTGACTG AAGCCAGCCT CAGTTTTGTC CTCTGTGATG TGAGGACTTG 240 AGCAAGAACC TTGCCAAAGC TCCCCTAGCC AGGATACTCT ACAATTGCAC ACCCCTGGCT 300 TCAGGCCTCC CCAGGGAACT TTACCTCCTG GTGAGAAGGG GTTGTGGGCC AAGATCTGCT 360 GGCAGCAGAG CTCCCCAGCA TGGGCCATTA ATCCACATGG GGACAGTTAG CATAACTGAA 420 ATTTAATCAA ATAAATGGCT AAAACTTAAT TGTTAAGTGG GAGTTTGCCT GTGCCATCTC 480 ACAGATGGCA TGCTCCCTAA TCCTACAGCT TACTGCACGG CTAGACACCA TCCGAGGGAC 540 AGGGTAAGAC CGAGACAGCT CCTGCTCACC TCCCAGTTGG CCCCACACCA TGCACACTCA 600 GGTCCTGGTG AGGCCACTTG TCACCAGAAG GCCCATTATG CTAACATGCA ACTAAGATAA 660 AATGGATAAC TCTTAAGGGG GCAAAAGATC CCTCGTGGGA AAGGCTCATG GTAAGAGAAC 720 GCACCTCCCT GGAAACAGAT GTCTTGGTCC TATAACACAA ATTGCAGTAT CACATCCCCA 780 AAACACAAGC CCTCCCATAA ATCATTCAGG GGAGCCTGTT TCGTTTTCCT GTTCTGATGA 840 AAGTGACCTG CATGTGGGGC TCAAGGCCAA AAGCACTGCC ACACTCGAGC AACTCCACAC 900 TTCCCCACGG CTTACTGTAA AGATGCTGAC CAAAACCACC AGGGCTGGAA CCGCTGCCCT 960 GCCCAACCTG TAGAAGTTGG CATTCCCCAG GGTTCTGCCC ACAGGCTGAG CCCCTGCCCT 1020 TCCCCCTCCT CCTTTGCCAA TCCTACCAAG TGCTCAATGC 1060
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