| Tag | Content |
|---|
EnhancerAtlas ID | HS074-01222 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr1:204430070-204432690 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:204430535-204430556 | AGAGGAGGGGCAGAGGGAGAA | + | 6.85 |
|
| | Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
| SE_00064 | chr1:204429083-204439520 | Adipose_Nuclei | | SE_01898 | chr1:204432147-204436806 | Aorta | | SE_03188 | chr1:204430961-204431525 | Brain_Angular_Gyrus | | SE_03188 | chr1:204432108-204432739 | Brain_Angular_Gyrus | | SE_03975 | chr1:204428687-204432015 | Brain_Anterior_Caudate | | SE_03975 | chr1:204432055-204439410 | Brain_Anterior_Caudate | | SE_04850 | chr1:204428109-204440381 | Brain_Cingulate_Gyrus | | SE_05834 | chr1:204428180-204440061 | Brain_Hippocampus_Middle | | SE_06778 | chr1:204428166-204440350 | Brain_Hippocampus_Middle_150 | | SE_07775 | chr1:204428249-204440457 | Brain_Inferior_Temporal_Lobe | | SE_10255 | chr1:204428606-204432650 | CD19_Primary | | SE_10905 | chr1:204414650-204438582 | CD20 | | SE_26688 | chr1:204429951-204431942 | Esophagus | | SE_26688 | chr1:204432283-204434113 | Esophagus | | SE_30246 | chr1:204429678-204437104 | Fetal_Muscle | | SE_31610 | chr1:204430030-204431806 | Gastric | | SE_31610 | chr1:204432232-204434041 | Gastric | | SE_40776 | chr1:204428531-204437031 | Left_Ventricle | | SE_42225 | chr1:204428390-204439096 | Lung | | SE_48746 | chr1:204429089-204432007 | Right_Atrium | | SE_48746 | chr1:204432136-204436808 | Right_Atrium | | SE_49909 | chr1:204428267-204431997 | RPMI-8402 | | SE_49909 | chr1:204432030-204436617 | RPMI-8402 | | SE_50149 | chr1:204429244-204432000 | Sigmoid_Colon | | SE_50149 | chr1:204432208-204434072 | Sigmoid_Colon | | SE_51536 | chr1:204429613-204432149 | Skeletal_Muscle | | SE_52421 | chr1:204429319-204432028 | Small_Intestine | | SE_58430 | chr1:204415099-204506026 | Ly1 | | SE_59794 | chr1:204415680-204491493 | Ly4 | | SE_61475 | chr1:204430067-204500813 | Toledo | | SE_62377 | chr1:204415291-204492168 | Tonsil | | SE_65868 | chr1:204430139-204431482 | Pancreatic_islets |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 5 | Chromosome | Start | End |
| chr1 | 204430292 | 204431282 | | chr1 | 204430759 | 204431008 | | chr1 | 204432329 | 204432499 | | chr1 | 204432124 | 204432239 | | chr1 | 204432250 | 204432649 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I204460 | chr1 | 204429650 | 204437135 |
|
Enhancer Sequence | TCCAGGGCTG GGAACTGTTG GAGAGAGCGG GGAAACAGAG GCACATCACA GGGAGCAGTT 60
GCTGAAGCCC TATCTTCTGG GCCTCTGTAT AGGGGACAAC CAGGAAGAGA CATGTTGGAG 120
TCCACCTGTG CTCAGGCTCC AGGGTGGGAG CTCAGCGAGA GACCCCTCTT CCAATGCTAC 180
CAACTAGGGT GCTGAGGCCA AAAAAACTTG GGGCAAGCCT ACCAAGCCTC CAGATCAGTG 240
TCCCCACCCA ACTTCTTTTT CTGCCTTCCA TCTGTTGGCC CTGCCTGCTT GTGAATAACC 300
TTACAAATTT CTATGACTTC TTGAAAAGTC CCAAATGCAT GCCAGTCCCA CCTGCTCAAG 360
CACCCATGTG TGAGACTCCC CCTTTCAGAG AGAAGGCCTA GGAGCCCTCG GCGATCCAAC 420
CTCTTCCTCT CTCCCAAATC ACACCTTCAA CAGCAAGGAA ACCCAAGAGG AGGGGCAGAG 480
GGAGAACTAC CTCCAGGCCA GCACTGCAGG CCTGGGCCTG GCCTCAGCAG CTGGGTAACA 540
GAAGCCGGAA AAGGACTTCC TTCCTCAGCA GAGCTGGGAA TCTAGGCCAG AAATGGAGAG 600
GAGAGGACAG GAGCATAAGG GGGGCAGTAT ATGTAAAAGC TGGCGGAGGT GCAGGGCCCA 660
GGGTCGTCTA GGTCCCATGA GGGCTCGAGT GAGGGGTTCT CCACATCCTG AGAGGACCAA 720
ATCTCCGATC TAGACCCTCT CAGATCTAAG ACTGAAGTGC AGCCAAAACC TGGAGGTGGT 780
GAGGCTGGGC TGTGGGGCTG GGCCTGGTGG GAGAGCCTGG GAGGAAGGAA GAGTGTGGTG 840
GGGCTGGGGG AGGTGGCAGG AAACCCAACC CTCCCACGGG ACTGCCTCAA GGTTCTTATC 900
TGAGAGCAGC CTGCATCCTG AACCCACTCA CCCCCTCAGT ATCAGCCCCT CCTGCCAGGC 960
AGGGGTAGAA AATCTCAGGG CTTCCTTGGG AACTAGCAGA TTTCTGGAAC CCCCGGAGCG 1020
TCCTTTCCAC CCCCATCCCA GGCAGTTGTC ATGTGTTGGG GGTCTGGGGG CTGGGCCAGG 1080
AGACAGCATT GTGCTTTTCT GTTGGGTGGG AGTGGGGCTC CTAGGCCAGG AGTCATGCAC 1140
ACAGGTCCCC TGGGGACTTG CTTGATCTTC TCTGTGGAAG GCCTTCCTCT CTGTGCATTC 1200
AAGTGAGAGT ATGAGGGGTG TGATCTGAGG ACCGCTGACC CTGTCCCACC TCACTAAGAA 1260
TATTTCACCT GAGTCTTAGC AGGAAGGTAG AACTTGACAG CTCCCACTAC CTCCGGACCC 1320
AGGGGCTCCA GGATTTGGGG TGCTGCAAGG GAAATGGCAG TATCTGTGCA GCCCAGAGCC 1380
CTAGGACTTC TCTCCGTGGG CTGCTCCTTC CCTGCTGGTA TTTACTGATT GCTCACAGGT 1440
CATTCTCACA TTTCACCCTC ACTGCAGCTT ACAGAGGGCC CTGAGCATCA ATCAGCCTTC 1500
ACAACTAGTA AGTGGCAAGT CCGAATTCAA ACCTGTGTAA TGGCGTCAGC AGGAGCTCCA 1560
ACTTATCCAC TATGTCCCCT TTTTCCCTTC TAACAGTGGC AGGCCACCTG GCACTCTCTC 1620
TGCCAGGCAA CCCTGAGTCT AGGACCCCTC CTGTTCCTCT AGGGGAAAAG TGTGTACATA 1680
AGTGAGTTTA AAGGTGGGGC ACATTTGAAG GGTACCCTGG AGTTGTACCA TACAGAACCC 1740
TGCCTCTTTC CTTTCCCTTA GCTTCGAGAT GAGGAGGCAG AGGCCAGAAA GGACCCCACA 1800
ATATCCTTAA ATTTGAAATA AGCCCAGATA GCTGGGCACA GTGGCTCACA CCTGTAATCC 1860
CAGCACTTTG GGAGGCCAAG GCGGGCAGAT CACCCGAGGT CAGGAGTTCG AGACCAGCCT 1920
GGCCAACATG GTGAAACCCA GTCTCTATTA AAAAATACAA AAATTAGCCG GGCGTGGTGG 1980
TGCTTATGCC TGTAATCCCA GCTACTCAGG AGGCTGAGGC ATGAGAATCG CTTGAGCCTG 2040
GGAGACGGAG GTTGCAGTGA GCTGAGTGAG ATGGCGCCAC AGCACTCCAG CCTGCACGAC 2100
AGAGTGAGAC TCTGTCTCAA AAAAAGAAAG AAGTCCAGAA ATGAATCTTC CATCCTGACT 2160
GCCAAATCTT ATGCTCTAGA CATAGATCAA CCATCCTTGC ATCTAGACCT GAATGTAAGA 2220
GAGAGAAAAA GCAAGCAGTG GCACTTATAG GGCACTCCTA AGAAGTGAGA CACAGGTCTC 2280
TCCTTTCTCT ATTCCCAAAA CGTGCTTCCT CCAAGTGGAC AGAGACTGGG GGCAGGAGCG 2340
GCTCTGAAGC CTAAGAGAGG AAAGCAGATC TTATCTGTCT GCTGTCACAC AGCTGTACCA 2400
TCTGAGAAGT GATAACCTTG CCCCTGCCTC TCTTCCACTG CAGCCCTCCA GAGCCCAGGG 2460
TAGTGGAAAG GGGGTTGCCT CAGCTGGTCC ACATCAGACT TTCCAGGGAG GCTGCTTTCC 2520
AGAGAGGGCA CTGGATGGAG AGGAGCTGGA GGCACGCCTT TGGGAGGAGG ATAACTAGCT 2580
GCACGGGCCA GCTGGGGAAA AGACTTGTTG GCAGGAGAAT 2620
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