Tag | Content |
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EnhancerAtlas ID | HS010-01003 |
Organism | Homo sapiens |
Tissue/cell | B_cell_blood |
Coordinate | chr12:4273450-4274740 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NKX2-3 | MA0672.1 | chr12:4274721-4274731 | TTCAAGTGGT | - | 6.02 | 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 |
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| 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 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I004164 | chr12 | 4273272 | 4275018 |
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Enhancer Sequence | GCTCCCCAGG ACAGCGGCTT CCTAGGGCTG TCTCTGTGCA TCTTCAAGGA GGGCGACTTC 60 TTGGTTCAAG TCCCAAGCTC ACCTCCTTGC TTCCATTCTC AGGTTGGTCC CCAGGGCGTG 120 AGACACACCA ACGCTCCCAT TCCCTCTAGT TTCTCTCTTT CCCCCACTTT CTCACTCGTT 180 TCAAGAGAAC GTTCCTATCC AGCGAATTTG TCATCATTTT CACTGCCTGG GTAACAACCA 240 TCGCAGCTGC CTTTTTTTTT TTTTTTTTTT TTTCTTGCAG GGAATGGGCC TGGAGCCGTG 300 AGCCGTCCCC TTCGCTAACC CCCAACCCCG CCTTCTCCTG CTCCTCCTCT CTTCACTCTT 360 CCTGCCTCTC GGCTCCGGGG TCTCCTCGCT TCCCCGCAGT CCCCGCCCCC CAGTTCCCAA 420 AGCGGCACCC GGGCCTCGCC TCCTTCCAGC GGAGCCGCGC GCCCTGCGTC CTGGCCTCCC 480 CGCCCCGAGT CCCCTTCCCT GGAGCCTGGG GGACCGACAG TCGCGGGCCA CGCACGCGGT 540 CCCAGCCTCG CCGTCCGCCC CGGGGAGAGC TGGAAGGTGG GCCCGGATCT CCCACATCAC 600 TATGAGCTCA TTCCAGCCCC GGCCAAGCAA AGCCTGGCCC TACTCGCTCC ACATGCATTT 660 CAGTCTCCTC TCGCCTTTCA TGCGCGGAGG AGCCGGGAGG GAGAGGATGT GACCTCATCT 720 GCGCGGCATC TGAGCCCAGG GGTGCCCCAG CTCTTCCACC CAGGCCGCTC CCCGAGCCCA 780 GCTCCCCGCG CCCCTCTCTC TATCCAGGAG AGACGCATTG GACAGCCAGG AGGGCTCGAC 840 GTGGAAGGAA AGGAAGCTGC AATTCTGGGA CAGGGGCAGA CGGGAGAGGA AGTGAACGTG 900 GCTAAACGCT CACTTTATGT AAAACGTCCC CCAGACTAGA ATCTCGTCCA CAGAGCTGCA 960 CACATACACT CGCACGGGCC CGGCTTGTAC TCAGGCAGGC ACACTCGCCC CCCGCCGTCC 1020 CCACCGCATC CCCCATACCC GTCCTAACTC ACTCCAGCCC CAATACAACC AAAAGGCATG 1080 AATTCAGGCG AAGGCGTTTT CTTCCCCATT TCCTCCTCAT GGCAGCAACG GAAACCTGAA 1140 TCTCAGAGCT GCCATGGGAC CAGGGGGCCA ACAGACCAGA GGCACCATCC TCAGAGCCCC 1200 CGGTCTGCCT GGGACTGGGA GCATGGCTGT GGCGCCCAAT GAGAACATAG TGTCCATAGT 1260 GACCATGATT CTTCAAGTGG TGTCTGAATT 1290
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