| Tag | Content |
|---|
EnhancerAtlas ID | HS177-03297 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr10:101725600-101726630 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT1 | MA0137.3 | chr10:101725850-101725861 | TTTCCCAGAAA | - | 6.02 | | STAT3 | MA0144.2 | chr10:101725850-101725861 | TTTCCCAGAAA | - | 6.32 |
|
| | Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
| SE_02745 | chr10:101725447-101726486 | Astrocytes | | SE_36644 | chr10:101725419-101726751 | HMEC | | SE_37968 | chr10:101721061-101728981 | HUVEC | | SE_44228 | chr10:101725677-101726732 | NHDF-Ad | | SE_45730 | chr10:101722085-101727174 | Osteoblasts | | SE_47277 | chr10:101720491-101728480 | Panc1 | | SE_64425 | chr10:101725390-101726915 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH10I099962 | chr10 | 101722359 | 101728672 |
|
Enhancer Sequence | TCAACATTTC ATTTACAGAC ACACTGATCT AATGGAAAAA GTGATTTTCA GTCTAGGAAG 60
TTGAAGCGCC ATCCCAAGCA CTAGACTTAA AAAACAGGAA ACCTAGATGC AAGTCTGATA 120
AACTTGCATA TCTGGCATAA AACAATACTT TCATTTTTTA GTGATTTTGT TTCCCACCAG 180
TAAATACCTG TTGATGTGAC TTGTCACGTA TACAAAAAGA GAAATTAAAA TCATTTGTGC 240
ACAAGCTAAG TTTCCCAGAA AAAGGCAAAT TGCATAGGTA TAACTAACTT CTCCATCCTC 300
CAAGCCTTGT GTTTCCAAAT TAAAAGACAG AGCTAAAAAA AAAACGTGAA AGGCATAGAA 360
GGAAAGCTGA CTGGTCAGTG TGTTTACTGG CAGTAGATTA TCACAGAGAG GAGAACAAGA 420
TAAAACCATG GATAATTAGT ACATCTCATT CTAGTCTCTC TTTCCCAGTG TATCCCCCTG 480
CCCACATCCT CTTCCTTTGG ATTCCACTTA CATCTTTAAG CTTATTAGGC TTAACTGGTT 540
AAAAGGTAGT CAAGATAAAA TCTAGATTCC AGGTCCTGGC CTGACCTTGA GTCAGTCTTC 600
AGACAGGTGA CTCACGATGC CAGATTCTTT CTGAGAATCT CTCGGATGGC ATGCTTCCTA 660
AGAAAAGTTC ATGCTACCCA CATCCTCTGA ACAGCTCAGC GGAAGCCACT GTACTCTTGT 720
CCTTTCTCCA TTCCATCAGA TATGGACTAC AGACTCCACT GGGAGAGCTA TGAGTAAGGA 780
CAGATAAGGT CCCTGCTATA ATCTCTTAAT CTATTTCTGT CTACCTTCCC AACACTGATT 840
AACAAGAAAG CATAGAGCTG AAGTAGAGAC TGAGTATAAA GTGAAGTGTA AGAAACTCTC 900
AAAACAACAG AGCGTGGTGG CGTTTTCTCT CGTTAATACG TTTTGTTTTT TTTTTGAAAC 960
AAGGTCTTGT TCTGTTGCCC AAGCTGGAGT GTAGTGGCGT AAACACAGCT CACTGCAGCC 1020
TCAACCTCCT 1030
|
