| Tag | Content |
|---|
EnhancerAtlas ID | HS093-20319 |
Organism | Homo sapiens |
Tissue/cell | HL-60 |
Coordinate | chr21:45615490-45617620 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SPI1 | MA0080.4 | chr21:45616347-45616361 | TGCTTCCTCTTTTC | - | 6 | | SPIC | MA0687.1 | chr21:45616347-45616361 | TGCTTCCTCTTTTC | - | 6.1 |
|
| | Number of super-enhancer constituents: 25 | ID | Coordinate | Tissue/cell |
| SE_00694 | chr21:45616149-45617521 | Adipose_Nuclei | | SE_03880 | chr21:45616016-45617515 | Brain_Anterior_Caudate | | SE_04775 | chr21:45609944-45617953 | Brain_Cingulate_Gyrus | | SE_05779 | chr21:45610164-45618120 | Brain_Hippocampus_Middle | | SE_06690 | chr21:45610194-45617897 | Brain_Hippocampus_Middle_150 | | SE_07737 | chr21:45615485-45617603 | Brain_Inferior_Temporal_Lobe | | SE_10305 | chr21:45615103-45617503 | CD19_Primary | | SE_11616 | chr21:45614519-45618143 | CD20 | | SE_24239 | chr21:45615918-45616296 | Colon_Crypt_2 | | SE_24239 | chr21:45616358-45616947 | Colon_Crypt_2 | | SE_30176 | chr21:45612703-45617986 | Fetal_Muscle | | SE_31647 | chr21:45615831-45617002 | Gastric | | SE_31647 | chr21:45617022-45617833 | Gastric | | SE_40890 | chr21:45615577-45618069 | Left_Ventricle | | SE_42286 | chr21:45615697-45617796 | Lung | | SE_48538 | chr21:45614456-45617946 | Psoas_Muscle | | SE_50113 | chr21:45615772-45617519 | Sigmoid_Colon | | SE_51445 | chr21:45609930-45618288 | Skeletal_Muscle | | SE_52463 | chr21:45615642-45617687 | Small_Intestine | | SE_59125 | chr21:45557380-45640832 | Ly3 | | SE_61237 | chr21:45557180-45641526 | HBL1 | | SE_61527 | chr21:45545883-45641600 | Toledo | | SE_62281 | chr21:45556124-45641130 | Tonsil | | SE_65639 | chr21:45615968-45617001 | Pancreatic_islets | | SE_65639 | chr21:45617003-45617940 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr21 | 45615654 | 45615733 | | chr21 | 45615635 | 45617233 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH21I005064 | chr21 | 45615830 | 45617229 | | GH21I044192 | chr21 | 45612024 | 45617843 |
|
Enhancer Sequence | GATCTGGGAC ATTCAACACC ATCTTATAAA AGATTCATAG AATACACATT CACACACCCA 60
CAAAAATCAA GAGAGCAGAT TTTCCAAAAA TAGGTGCAAG AAAGATCCAA CTTCCAGGAT 120
AAAATTTTAG AACCAACATT TCCATTAGCA AAAGCGGTCT TGTCTAAAAC TCTACCGACC 180
GCGCTAAAAT CCCATTCAAA ACAGAGCTCT GGTTACGTAG ATCGTGATCA ATAATGAGAA 240
ACTGTGAGGC GTCCCCGTGG GATCTGACAC TTCCTAGGGG AGCTTCTCTC CACTGGTAAT 300
AAAGATATAA TTAGGAATTT CAACTACCTG TGATTTTGCC AACTTACGGC ATTTGTTGAG 360
AATTTCGGTC CCTGTGTTTA TGCACACACC TTTCAACCTT AGATTTGACG GTGATGGGTT 420
AGTAAATGTC AATTCTAAAG TGGTCGTTTT CAACCAGGGG CAATTTTACC CCTCAGGGGA 480
CACTGGCAGT GTCTGGAGAC ATGTTTGGTT GTCATGACTT GGGGCAGAGG TGCCACGGGC 540
ACCTGGAGGG TGGAGGCCGG GGTGCGGCTC AATACCCTAA CCACACAGGA TGGCCCCAGG 600
ACAAAGATGC CCCTGGTGCT GAGAGCAGGG CCCTGTTCTA AGAGATGGGT GGCTGGAGCC 660
TGGCTGGAGG GCACTAGTGG CACTCTGGGC TGGTCTCCCA GGGCCCCATC TGCCAGGTCG 720
GGGGCCCACG TGGGCCTGCA GGATGTGCGT GCTTCTCTGC TGTTGAGATT GCATCAGCAC 780
AACAGCCACA GCCGTGACAC GGGGGCAGGC ACCTCAGTGA CGCCAGAGTC GGGGCGGGAG 840
GTGTGGAGAT CTGGGCTTGC TTCCTCTTTT CAGTCCCAGG ACAGCTCCTC TTTGGCTGTG 900
GGAGGCCCAG CTTCAGCCTT GTCTGTGGCT TCCTGGTGGG AGGACACAGG CCTTGAGGGA 960
CGTTTGTCCG AGACGGTCCT CATCCTACTG GTAGGGACAC AGAGCACCTG TTCCTCTGGC 1020
CCCTCCAGGA GCAAGACACA TGCACTGCTG AGGCCTTGGA AGCCTACACA GGTTTATCAC 1080
CCACGGCCAG ACCTGTCTGT CAGGGAGCAG GTGGGGTCAT CCTGCCCTGA AGCACCGATG 1140
AGCTGATCCC GGTCATGCAG AGTGGGTGGG GACCTCTTGG CTGGGCCTGT TCATGTAGCA 1200
CACACGGCTT TGCTGCCCAT AGAATCCAGG GCCCCCAGTG TGAGCACCAC TCTCCATCCC 1260
TGAGGCCGAG CCTTACCCTG GAGGCAGCCT CAGGTGAGAT GCCCCTAATG GAGCCACCTG 1320
GCAATGGACC GCTCTCAGGT CCTTCAGCTC GGTGCACTCA CCCGGGAGCC CTGCGTTCTG 1380
TCCTGGGGTA GAGGCTCAGG GTTGGTTTGA AGCCATATAG TCAGCTCCCA GAGTCACAGA 1440
AACGTCCAAG GAAGAAAACT GTCCGATTAC AGACTTTTAA AATTCATTCA TAGTTTAATC 1500
AAGAGAACTT GCTGTTCCTT CCTCAAATTT CCTAGAATTG GTCTTCTCAT AATCACCACC 1560
TAGGGCACAG CTGTGGCCGA GGCTCCCATG ATGAAGCGTC TGTGTCAGCG CTGACGAGGT 1620
CTGCCGAGGA CGCGTTTCTC TCTGCAGCCC GGCACCAGTC TCAAGGCCAT CGGCTCCGAC 1680
AGCGTCACCT CCTGGGACCT TCCCTTCATG TATGGTCCCA GCGGCATGCG GGCCTGGTGG 1740
AGGAGGTCCT GGCCTGCCGC CCAGGGATGG CCGGTCCAGG CGCAGGGCCG ATTGTCCACT 1800
TCTGGCCCCT GAGGTACCGG GAGGGCTGGT GAGCAGCATG TCTCGCTCTG AGACCGGCCA 1860
GGCTGCTGGG GCAGGCATCT GATGTACAGT AGTTCCCACA CGTGGCAATG TCACCAGCAA 1920
GAGCCACGTA TGATAAATTC AGGCCGTCCA CCGTGGCAAC ACTGGGAAGG CTGATTCTGT 1980
AGGAAAGGAT TGGCCTTGGG CCATCACTGT TCAAAGAAGA AGAAATCCCT GGATCACTGT 2040
CTGATCCAAC TCCAGACAGA CACTCCACAC AGGATTCCTC CTGGGGATCA CGGCTCTTCT 2100
CTTGGCGGAG AAGAAGGAGG GAGAATGAGC 2130
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