| Tag | Content |
|---|
EnhancerAtlas ID | HS162-00807 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr1:180182460-180183610 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | + | 6.02 | | BHLHE41 | MA0636.1 | chr1:180182706-180182716 | GTCACGTGAC | - | 6.02 | | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | + | 6.77 | | MITF | MA0620.2 | chr1:180182702-180182720 | CAGGGTCACGTGACTAAT | - | 6.77 | | USF1 | MA0093.2 | chr1:180182705-180182716 | GGTCACGTGAC | - | 6.14 | | USF2 | MA0526.2 | chr1:180182702-180182718 | CAGGGTCACGTGACTA | + | 6.66 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 180182841 | 180183144 | | chr1 | 180182549 | 180183199 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I180213 | chr1 | 180182536 | 180182962 |
|
Enhancer Sequence | TTGCTACTAT AGACGCTTAG ATGTTTGAAT TATTTGCAAA GCATGTGTAT TACTTCTGCA 60
AGAAAAATAA AATAGGGAAA ATTTCTACTT CAGCAAAACG ACTATCTCCT ACTTATCAGA 120
GCATTTCCAA GTCACTCACA CATATTTGAA CATTTGAATG TTAAGTCCAA GAACACTGGC 180
AGAGGCAATC ATGCTCCCGC CAGTCCATCG GCTCCCCAGA TTTTCAGGCT CCAGCCGGGA 240
GTCAGGGTCA CGTGACTAAT TCTAGCCAAT GAGATGGAAG CGAGCGCCAC CTCCCGGAAA 300
GGAAATGATG CCCGTAACTT AGAGCGGGCT AAGGTGCTCA ACTCTCCAGT TTCCCTTCGT 360
CTGTCTTGGC CACAAAGGAA ACCACACATT CTAGATATAA AATGTTAGAG CCACCTGCCA 420
AACACTGTAC TTTTGTTATG CCACTGAGAT TTGAGGGTTA ATCTGATGCG GCATTGTATT 480
CTGGCCTATT TCAATTCTCT ACTGCTATCT GACAAACCAC CCCAAAATGT CTTAGCTTCA 540
AACAACACTC ATTTTCTTTG CTCATGACTC TGCAGTCTGG GCTAGTTTCA GCTGGGCAGC 600
TCTTCTGCAG GTCTTGCCAG GGTCATTAAT GTGGCTGCAT TCAGCTGGCG GGCAGGCTGA 660
AGGCTGGGCT TAGCTGAACT CACAAGACAG CTGGGCCTTT CTCTCCCCAC CCCCGTCTCT 720
CTCCCCACTC CCCGCCATAT AGTGTCTCCA CAAGGCCCAA GGTCTCTCTG GTAAAGTAGT 780
TGGACTTCTT GCACAGATGG GGGCTCAAAG CTCCCTAAAG TGCCATGCCA TCTTAAAACT 840
TAGTCCCAGA ATGGGCACAG TGTTACTTCT GGTACCTTCT GTCGGTTAAA GCAAATCACA 900
GGTCCAGTCC AGACTCAAGA AAAAAGGACT CCACAAGAAC ATTCAAATAT CAGAGATGTG 960
GTTCATTGGG GCCACCTGTG CAACACAGTG CCATGGCCTC TTCTGAGCAG TATAAACACC 1020
AAGGGCCTAC TCCATATGGG AGAATGCTGT GTTGCACACA TAATGTTGTG TAATCTTTTT 1080
TTTTTTGAGG CAGAGTCTCA CTCTGTCGCC AGGCTGGGGT GCAGTGCACT GCGTGATCTC 1140
AGCTTACTGC 1150
|
