| Tag | Content |
|---|
EnhancerAtlas ID | HS103-03771 |
Organism | Homo sapiens |
Tissue/cell | HUES64 |
Coordinate | chr11:9058140-9059760 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr11:9059513-9059528 | TGCCCTTTGCCCTCT | - | 6.01 | | NR2C2 | MA0504.1 | chr11:9059513-9059528 | TGCCCTTTGCCCTCT | - | 6.56 | | REST | MA0138.2 | chr11:9058305-9058326 | TCTGCTGTCCCTGCTGCTGAG | - | 6.28 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr11 | 9058455 | 9059015 | | chr11 | 9059105 | 9059442 |
|
Enhancer Sequence | ATATGGTGAC AATGATTCCA ACAGCCCCAT TAATCATAAC GTAGAGTCAC ATCACCATGG 60
TCTGTTCCAT CATGGTTCCT CTGGCAGAAA ACAGATGTCC TCAGCAGGTG GACAACACCA 120
GGCCTGGTTC TCACTGAGCC AGGGACCAGG ATGGGCTCCT GCTGCTCTGC TGTCCCTGCT 180
GCTGAGAACT CTTTCAACCT CCACAGCCTT TGCAAGGTGA CCTTTAGAGA GACCTCACAA 240
TATCCCACCT CTGTGCCATT TCTTAACTGC TCGAAGTGCC AAGAAACCCT TCAGGCTGCC 300
CTGTGGAAAA GAGGGCACCA GTTCTTTTTC CTCACAATGA AAGGCCTGCT TCACATAAAC 360
AAACTCATAT TGTCAGTCAC AGTGTCCATT TTCCTTCCAG AGAGAAAGAC CTGCAGAAAT 420
AATTCATGCC AAGCACCTCC CAAATATATT TGATTCTTTC ACAAGGTAAA AATGAGCTAA 480
ACACTAAAAG GCAACTCTGA AATATCATGA AGGGATGCCT GAAAACCGCT CTTTGCAAAT 540
GTGCTGAGAA TCTGGCCTGC AGAGACCTCA ATCACACGTT CCAGTGGCTT CTCTCTTCTC 600
CTTCAGCAGC CAGCTTGTTT TGCTGCCCAG GACAAAGGAG TCAATTGCCC CCAGAACACT 660
TCACTATCAC AGCAAAGCTT TTGTGTGCCT TCAGTGACCA TTAAAATCTC ATTCTCAAAT 720
CCCACACAGC TGTTTTTTCT CCTTCTTTAA AAAAGATACG AGAAAGCTTT TCTGATGCAA 780
AAGGGACAGA CCAGCAGGAT GAGGATTAAT GGCGACAAAG AAGCTTGAAG CCTCCGCCTC 840
TTTTCAGCAC TGTGGCCTTT GAGTATTTCA GGCTATAGAC AAACACTATG GTCTCTCTGT 900
GGCTAAGATG ATGAACCTAA TAAAAGGGGT CACCCTCTAG TATTTGACTG CTTTCTTAAG 960
AATCACGCCT TGACTTCTGA AGAAGAGCCA TAAGCAGCCC ACGTGGATTC CCAGGGTGCC 1020
CCAGGGCTGC TGCTTTGTCC CAGTCCAGAG GTGCTGATGC CCCAGGCAGA GTTGGCCTCA 1080
GGATCCTGGT TTGAGCTCTC TTTAAATGAC TGCCCCCATG ATAACAGGGG ACAGTCCTTC 1140
TTGGGCTGAG AGATTGATTT TTCATTGTCC AGGTTTTTGA CCTGTGCTCA GGTTTGCTCT 1200
TTAAAAACAT TCCTGTAGTT GAGGCAGAGA AATGAGCCCA GCTTGATGCC TTCTTCCTTA 1260
TTGGGTTCCC AAATGCACAC TATGTTCTTT TCATGCCTAG TTAACTGGAG CTGAAATTTC 1320
ACTTCCTTTA GAGTGCCTTT TTTGCCCTCA ATTTAAATAT TTCTCCAAAG ATTTGCCCTT 1380
TGCCCTCTTT TCTCTTAATG TTATCTACTA TCCTTGGGAT TTCATCTGTT GTCCCTGTGA 1440
AGATTCATTT ACTCATTCAT TCAATAAGTA CTTATTGAGC ACTCATTATG TGCTGAGTAC 1500
CGTTCTAGGA GCTGGAGACA CAGCAGAGAA GAGACATGAC CCTGTTCTAA TGGGGTTCTC 1560
AGGGCAGTAA ATAAATGAGC AATAAATCTC AATGAGCAAG CAAATAAGTA TGTAATAGAA 1620
|
