| Tag | Content |
|---|
EnhancerAtlas ID | HS162-05628 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr2:99485970-99487090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr2:99486233-99486254 | CCCCAGTTTCAGTTTTCTTTT | + | 6.93 | | KLF4 | MA0039.3 | chr2:99486427-99486438 | CCACACCCTCC | + | 6.32 | | Klf1 | MA0493.1 | chr2:99486425-99486436 | GGCCACACCCT | + | 6.32 | | LBX2 | MA0699.1 | chr2:99486995-99487005 | GCCAATTAGC | + | 6.02 | | Mafb | MA0117.2 | chr2:99486630-99486642 | AGTCAGCAGTTT | - | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_24439 | chr2:99484486-99486777 | Colon_Crypt_2 | | SE_24439 | chr2:99486827-99487673 | Colon_Crypt_2 | | SE_27533 | chr2:99484074-99487516 | Esophagus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr2 | 99486926 | 99487008 | | chr2 | 99486600 | 99486798 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I098867 | chr2 | 99484176 | 99487382 |
|
Enhancer Sequence | TGCTCACCAT GGAAGCAGGC AAAGGGCAAT GGCAGGTGAG GCTGCATTCC CCATCTGAGG 60
AAGGGCAGGG CCCAGGAAGA AAGAGGAATG CTGAGAAAAT CGGAAACAGC TTCTGAGCCA 120
GACACACCCA GGCCCAGGGC TCTCCTCTCT CATTCCAGCA CCAAAACCAC CCGGCCCCTC 180
CTGCCTCGCC TTGATGTCCA CTTGCTATCT CAGTGCGAGG GACCCTGTGG GAGGCACGCT 240
CGTCTCTGCG CTGCACACTT GCTCCCCAGT TTCAGTTTTC TTTTTACTTT TCCTTAAAGG 300
CCCATCGTGT TACCTCAGGT CCTTGATATG CTTTGTTAAC TGCTTTCCTG GGGCCTTCCC 360
AATGCTCCTT TACCAGGGAC CTGCTTGCCC CACTCATTGT TGCACTGATG GGATTTCCAG 420
CCCTCCCCCT GGAGCCCAAA CCTGACAGGT GCAGGGGCCA CACCCTCCCA AAAATCACCC 480
ACTGAGCCTG CCCAGCCGGC TCCCCAGCCA CCCCACGTGA CACAGCCACT TGCCCTGGTG 540
GCTCCTATCT GATTACCTGC AGCTGCCACT TCAAAATAAT AGACTCCTGC AACTGGCATC 600
ACAATGCCAC CTGACTCAAG TTCCTCCCAA GTCTGATGGC TTGCCAACTG CAACCGGTAC 660
AGTCAGCAGT TTCCAGGCAA TATCTGGAGT GTTGACAGAG GGCTCTGGGT GGCAGGTGCG 720
ATTCTATGTT AGTAAAACTC AGGAACAGGC AGCAGCAAGG GCAACTTCTG AAGATGGTTC 780
TGAAAAAGCC CTAGTTTGCT TTTCTGTTTT CCAAATGGCA ACTGTATATA GAATTCTACT 840
CAAATGGCCT ACAATTTAAT TTTAAAGCAC AACGAATACA TTTGATGATG ACAGAAGAAA 900
GCAGTGAGTT CAGAGGAGAG CTCAGATGAT AATCACGCAG TGCGCTGAAG GTAGTTTATA 960
TACATTTGCC CTTTGTGCAG CCCACTGTGC TCCTGCCAAC GACTTGGCCT TCTCCCAGGG 1020
AGAGGGCCAA TTAGCTGGTG GAGAGTCCCC TGTATCCTGG GAGGTGGTGC AGGGGCCCCT 1080
GCAGCAGAAT GGATTATTGA AGGGACAGGG ACTGGGCCCC 1120
|
