| Tag | Content |
|---|
EnhancerAtlas ID | HS148-03835 |
Organism | Homo sapiens |
Tissue/cell | NHLF |
Coordinate | chr12:4273400-4274730 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr12:4274548-4274569 | TTCTTCCCCATTTCCTCCTCA | - | 6.13 | | ZNF263 | MA0528.1 | chr12:4274135-4274156 | GGAGGAGCCGGGAGGGAGAGG | + | 6.1 | | ZNF263 | MA0528.1 | chr12:4273779-4273800 | GCCTTCTCCTGCTCCTCCTCT | - | 6.45 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_10702 | chr12:4273459-4274966 | CD19_Primary | | SE_11778 | chr12:4273012-4275197 | CD20 | | SE_58886 | chr12:4216067-4279606 | Ly3 | | SE_61003 | chr12:4215547-4279853 | HBL1 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr12 | 4274113 | 4274463 | | chr12 | 4273400 | 4274000 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I004164 | chr12 | 4273272 | 4275018 |
|
Enhancer Sequence | AAATTGTCTT AGGGGCATGC GAAGGCCACC CTTCTGGTCT CCGCAGCTCC GCTCCCCAGG 60
ACAGCGGCTT CCTAGGGCTG TCTCTGTGCA TCTTCAAGGA GGGCGACTTC TTGGTTCAAG 120
TCCCAAGCTC ACCTCCTTGC TTCCATTCTC AGGTTGGTCC CCAGGGCGTG AGACACACCA 180
ACGCTCCCAT TCCCTCTAGT TTCTCTCTTT CCCCCACTTT CTCACTCGTT TCAAGAGAAC 240
GTTCCTATCC AGCGAATTTG TCATCATTTT CACTGCCTGG GTAACAACCA TCGCAGCTGC 300
CTTTTTTTTT TTTTTTTTTT TTTCTTGCAG GGAATGGGCC TGGAGCCGTG AGCCGTCCCC 360
TTCGCTAACC CCCAACCCCG CCTTCTCCTG CTCCTCCTCT CTTCACTCTT CCTGCCTCTC 420
GGCTCCGGGG TCTCCTCGCT TCCCCGCAGT CCCCGCCCCC CAGTTCCCAA AGCGGCACCC 480
GGGCCTCGCC TCCTTCCAGC GGAGCCGCGC GCCCTGCGTC CTGGCCTCCC CGCCCCGAGT 540
CCCCTTCCCT GGAGCCTGGG GGACCGACAG TCGCGGGCCA CGCACGCGGT CCCAGCCTCG 600
CCGTCCGCCC CGGGGAGAGC TGGAAGGTGG GCCCGGATCT CCCACATCAC TATGAGCTCA 660
TTCCAGCCCC GGCCAAGCAA AGCCTGGCCC TACTCGCTCC ACATGCATTT CAGTCTCCTC 720
TCGCCTTTCA TGCGCGGAGG AGCCGGGAGG GAGAGGATGT GACCTCATCT GCGCGGCATC 780
TGAGCCCAGG GGTGCCCCAG CTCTTCCACC CAGGCCGCTC CCCGAGCCCA GCTCCCCGCG 840
CCCCTCTCTC TATCCAGGAG AGACGCATTG GACAGCCAGG AGGGCTCGAC GTGGAAGGAA 900
AGGAAGCTGC AATTCTGGGA CAGGGGCAGA CGGGAGAGGA AGTGAACGTG GCTAAACGCT 960
CACTTTATGT AAAACGTCCC CCAGACTAGA ATCTCGTCCA CAGAGCTGCA CACATACACT 1020
CGCACGGGCC CGGCTTGTAC TCAGGCAGGC ACACTCGCCC CCCGCCGTCC CCACCGCATC 1080
CCCCATACCC GTCCTAACTC ACTCCAGCCC CAATACAACC AAAAGGCATG AATTCAGGCG 1140
AAGGCGTTTT CTTCCCCATT TCCTCCTCAT GGCAGCAACG GAAACCTGAA TCTCAGAGCT 1200
GCCATGGGAC CAGGGGGCCA ACAGACCAGA GGCACCATCC TCAGAGCCCC CGGTCTGCCT 1260
GGGACTGGGA GCATGGCTGT GGCGCCCAAT GAGAACATAG TGTCCATAGT GACCATGATT 1320
CTTCAAGTGG 1330
|
