| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08436 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:46928550-46929810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr13:46929131-46929145 | GGAAAATGACTCAT | + | 6.76 | | MEF2C | MA0497.1 | chr13:46929227-46929242 | TGCTATTTTTATCTC | - | 6.5 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_09573 | chr13:46925808-46930539 | CD14 | | SE_11021 | chr13:46926777-46931216 | CD20 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr13 | 46928720 | 46929572 | | chr13 | 46929409 | 46929462 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH13I046354 | chr13 | 46928293 | 46930078 |
|
Enhancer Sequence | ATCTAAAATT ATCTCAAAGA CAAAAGTTAA AAAAAATGTA TCCTAGAAGC TAGAGGAATT 60
TAACAGGAAA AGCCCAAAAT TATTTCTATG CTGTCTACAA TCTGGGCCCC GCCTACATCT 120
GCAGCATGTT TTCTCCTCCT ATTCTTACTC TCTGGCCACA CAGGGTTTCT TTTACTTGCC 180
ACAGGCCCTT TGCACATGAC GAACACCCCT ACTTCTGTGG GCAATCACTT TCCGATGAAA 240
CCTCTTACTC CCAGCTTCTC AAGCTCAGAT GAAGTTCCCT TGCTGTAAAT CCCACGGCAC 300
TCTTGACTCT TTTGTTACGT ACATCACTTT GTGTTACATA CACTTACTTG GCTGATGAGT 360
GTATCTTCCC TAAAAGATGA TAAGCAAGCT CCCTGAGGGC AAGGCCACTG TACAAAAGTG 420
CAGACACACA TCTCCATACC TGAACAAGCT TAGGGAAATA ACAAAAAGTT GGTGGAGCGA 480
TAGTCATATG TGTACAGTTT CTGACTCATG CATTCAATAT TTACAGAAGC GCCAGGATAC 540
AGTGGTTAAC CAAAGAGACA TGTTCCCCAC TAGATGTGCT GGGAAAATGA CTCATTCAAA 600
GAAAATCAGC AACAATGGTG ATGCCCGTCA GGCATTATCA TCCAGTGTAG GAGAGGAAGC 660
CCAGATCGAT TCCTGCTTGC TATTTTTATC TCTTGAAGTA GGAGCTCCTC ATAGTCTTTT 720
TCCTTCAAAA ACCGACTATC AAAGGCTAAG GGAACTCTTT CCACAAAGCT CCTCTTTCCA 780
GCCTTTTGCA GGTCAGACAT ACAGGTACCA TCAGAGCAGA ACAAGTGATT CCCAGTCTCA 840
AGGGGGAAAC TTGCATTTCT GACTGAGGAA AGCCCGAGCT TTTTTTTTTT TTTTTTTGAG 900
ACGGAGTCTC ACTTTGTCAT GCAGGCTGGA GTACAATAGT GTGATCTCGG CTCACTGCAA 960
CCTCTGCCTC CTGGTTTCAA GGAATTTTCC TGTCTCAGCC TCCCGAGTAG CTGGGATTAC 1020
AGGAGCCTGC CACCCATGCC TGGCTAATTT TTTTGTATTT TTAGTAGAGA TGTGGTTTCA 1080
CAATGTTGGC CAGGCTGGTC TCAAACTCCT GACCTCAGGT GATCCACCCA CCTTAGCCTC 1140
CCAAAGTGCT GGGATTACAG GTGGGAGACA CCGTGCCTGG CCCAGGAAAG CCTAATCTTC 1200
TAGGCCTCAG TTGGCCCAGG AATGATCCTC TCAGGCTACC TCCTCAAACT CTCAGAGAAG 1260
|
