| Tag | Content |
|---|
EnhancerAtlas ID | HS170-01049 |
Organism | Homo sapiens |
Tissue/cell | RS4-11 |
Coordinate | chr14:20895360-20896960 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NKX2-5 | MA0063.2 | chr14:20896137-20896147 | ACCACTTGAG | + | 6.02 | | SPIC | MA0687.1 | chr14:20895990-20896004 | AGAAAGAGGAAGCA | + | 6.04 | | ZNF263 | MA0528.1 | chr14:20895933-20895954 | GGAGAAAGAAGAGAAAGAAAA | + | 6.03 | | ZNF263 | MA0528.1 | chr14:20895930-20895951 | GAGGGAGAAAGAAGAGAAAGA | + | 6.42 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28028 | chr14:20895260-20896705 | Fetal_Intestine | | SE_29051 | chr14:20895241-20896718 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr14 | 20895383 | 20896384 | | chr14 | 20896422 | 20896678 | | chr14 | 20895931 | 20896136 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020426 | chr14 | 20894921 | 20897612 |
|
Enhancer Sequence | ATTAAAAAAA AAAAAAGAAA AAGAAAATTG ACCTAAACAC ACACAAAAAA ACTGACCCTT 60
TTTTGCTCTC AGCTGTCCAG TAGGCAGAAA TGGAAAGAGC AGACAGGAAG GATAGAGGTG 120
AGTCATAGAG GGCGGGAATA CACAATCATT AAGTGAAAGC CATTATCCTC AGGAAGGCTC 180
CAGAGAAGAG AGTAGGTGGC AAGAGCAGCA GAATTATCTG AAAAGCCTCT GGAATACCCA 240
CTTCCTCTTT GCTATGGAGA AACAGGGCAT GGCATGCCCC ACTTCTTTCT GTTTCAAATG 300
CATTCCCCCT TCTCTAATGG GTGAGACTCT AGGCAGCCTT TAAGATCCAG TTCAAAATAC 360
ACCCATCGGA TGACACCTTT CCTAACAGAA GCCTTCCTGA GCAGAGTTCA CTGCTCTATC 420
CTCTGGGCTC TCGCAAGACT CGTCCATACA TGTAAGTCCA CTCAAAATTT GTATTTGTTT 480
ATGTCTATCT GCTGGTCAGG AGCTCTCTGA CCTCTGTATC TTGGTGCCTC CTACAGTGCC 540
TGCCACACAG TAGGTAATTA ATAACTGTGT GAGGGAGAAA GAAGAGAAAG AAAAAAGAGA 600
GGCAGTGGGG AGAGCAGGAT GGGGGAAGAG AGAAAGAGGA AGCACCTGAC TACCTTCCCT 660
GGCCAAGATA AAGGGAAATG GATTTAAAAA TAACTCTGGG GGAAAGGAAC TGAAAGGGGG 720
AAATGACTTT TCTGAGTCTT GTCTGCTTCT CACTCTTCTC TCCCCCCACA TCCTCTCACC 780
ACTTGAGACC TCAGGCAACA ACGGTCTCAT TTTCACTCCT GATTCCTCAG TTTGCCCAAA 840
AGAAAGAAGG CACACAGGCT TCTGACTTCT TCCACCCCAT CTCCTTAAAC CTCAGATCAT 900
CTGTTTTTCC ACTGTGGGCC TCTCCCTCCT TGGCCTCTGC CCCCATCATC TTTCCCACAC 960
AACACTCCTG CCACATGGCC CTGGGGGGCC CGTCAGGCCT CTCAGGCCCC TGTGCCGTGC 1020
ATGTCCATGT GGGAGCTTCT GCCTCAGAAG GAAACCAAGA GGTTCTCAGG GGCAGCCTGT 1080
GGTGTCTCGC TGGGAAACGC TAGACCAGGC CTACAAAGTT ACCCGGGAGA GAATATTGTT 1140
AAGAAGGTTT AGGCATCCCA GGGGTGGGAG AGGAGAAAGG AGCAAGTTCC AGGAAAAAAA 1200
GGGCTGAACG ATTTACAGTC CTTACTCCTA CACTCCTCAA ACTCTTTCAT GGATGGCCAT 1260
TCCACATTTT TCCCATGATC CATGGGTCAG AACCATTTTT CCAACTGTCC TCCCATGGTC 1320
TCTACACTTT GGCTACTGAA GCTTCTTAAC TCTCTTTCAA ACTAGATGCC CTTTCCCTAA 1380
GAATCCCTAA GCCTTGTGGA GTTGCTCCCG AGTCTCCTTT CCTCACCTGG GTATTCAGCT 1440
GCCTCCCCTT TCCCTATATG TTTTCCCTAG GAGTTCTGGA ACCACCATTT CCTCAACGGA 1500
GATCATACGT ACAAAAGCAG TTTACAATGC ACAGTGTGAG AATAAAATAC TACCAAGAAT 1560
AAAGCCTCTT TTCACTCCCC ACAATCTCTG TCCTTCTCTC 1600
|
