| Tag | Content |
|---|
EnhancerAtlas ID | HS074-04285 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr14:20895320-20896960 |
Target genes | | Number: 10 | Name | Ensembl ID |
|
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: 4 | Chromosome | Start | End |
| chr14 | 20895335 | 20896697 | | chr14 | 20895383 | 20896384 | | chr14 | 20896422 | 20896678 | | chr14 | 20895931 | 20896136 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH14I020426 | chr14 | 20894921 | 20897612 |
|
Enhancer Sequence | ACCCTAAAAC TTAAAGTATA ATAATAATAA AATAAAATAA ATTAAAAAAA AAAAAAGAAA 60
AAGAAAATTG ACCTAAACAC ACACAAAAAA ACTGACCCTT TTTTGCTCTC AGCTGTCCAG 120
TAGGCAGAAA TGGAAAGAGC AGACAGGAAG GATAGAGGTG AGTCATAGAG GGCGGGAATA 180
CACAATCATT AAGTGAAAGC CATTATCCTC AGGAAGGCTC CAGAGAAGAG AGTAGGTGGC 240
AAGAGCAGCA GAATTATCTG AAAAGCCTCT GGAATACCCA CTTCCTCTTT GCTATGGAGA 300
AACAGGGCAT GGCATGCCCC ACTTCTTTCT GTTTCAAATG CATTCCCCCT TCTCTAATGG 360
GTGAGACTCT AGGCAGCCTT TAAGATCCAG TTCAAAATAC ACCCATCGGA TGACACCTTT 420
CCTAACAGAA GCCTTCCTGA GCAGAGTTCA CTGCTCTATC CTCTGGGCTC TCGCAAGACT 480
CGTCCATACA TGTAAGTCCA CTCAAAATTT GTATTTGTTT ATGTCTATCT GCTGGTCAGG 540
AGCTCTCTGA CCTCTGTATC TTGGTGCCTC CTACAGTGCC TGCCACACAG TAGGTAATTA 600
ATAACTGTGT GAGGGAGAAA GAAGAGAAAG AAAAAAGAGA GGCAGTGGGG AGAGCAGGAT 660
GGGGGAAGAG AGAAAGAGGA AGCACCTGAC TACCTTCCCT GGCCAAGATA AAGGGAAATG 720
GATTTAAAAA TAACTCTGGG GGAAAGGAAC TGAAAGGGGG AAATGACTTT TCTGAGTCTT 780
GTCTGCTTCT CACTCTTCTC TCCCCCCACA TCCTCTCACC ACTTGAGACC TCAGGCAACA 840
ACGGTCTCAT TTTCACTCCT GATTCCTCAG TTTGCCCAAA AGAAAGAAGG CACACAGGCT 900
TCTGACTTCT TCCACCCCAT CTCCTTAAAC CTCAGATCAT CTGTTTTTCC ACTGTGGGCC 960
TCTCCCTCCT TGGCCTCTGC CCCCATCATC TTTCCCACAC AACACTCCTG CCACATGGCC 1020
CTGGGGGGCC CGTCAGGCCT CTCAGGCCCC TGTGCCGTGC ATGTCCATGT GGGAGCTTCT 1080
GCCTCAGAAG GAAACCAAGA GGTTCTCAGG GGCAGCCTGT GGTGTCTCGC TGGGAAACGC 1140
TAGACCAGGC CTACAAAGTT ACCCGGGAGA GAATATTGTT AAGAAGGTTT AGGCATCCCA 1200
GGGGTGGGAG AGGAGAAAGG AGCAAGTTCC AGGAAAAAAA GGGCTGAACG ATTTACAGTC 1260
CTTACTCCTA CACTCCTCAA ACTCTTTCAT GGATGGCCAT TCCACATTTT TCCCATGATC 1320
CATGGGTCAG AACCATTTTT CCAACTGTCC TCCCATGGTC TCTACACTTT GGCTACTGAA 1380
GCTTCTTAAC TCTCTTTCAA ACTAGATGCC CTTTCCCTAA GAATCCCTAA GCCTTGTGGA 1440
GTTGCTCCCG AGTCTCCTTT CCTCACCTGG GTATTCAGCT GCCTCCCCTT TCCCTATATG 1500
TTTTCCCTAG GAGTTCTGGA ACCACCATTT CCTCAACGGA GATCATACGT ACAAAAGCAG 1560
TTTACAATGC ACAGTGTGAG AATAAAATAC TACCAAGAAT AAAGCCTCTT TTCACTCCCC 1620
ACAATCTCTG TCCTTCTCTC 1640
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