Tag | Content |
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EnhancerAtlas ID | HS037-03387 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:223925050-223926880 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr1:223926788-223926799 | AGGCACTCAAG | + | 6.14 | REST | MA0138.2 | chr1:223925234-223925255 | GCTCATGTCCAGGGTGCTGGA | - | 6.48 | STAT3 | MA0144.2 | chr1:223926464-223926475 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 31 | ID | Coordinate | Tissue/cell |
SE_00224 | chr1:223923747-223925516 | Adipose_Nuclei | SE_00224 | chr1:223925520-223928901 | Adipose_Nuclei | SE_01908 | chr1:223924719-223925413 | Aorta | SE_01908 | chr1:223926095-223926935 | Aorta | SE_02306 | chr1:223924738-223925366 | Astrocytes | SE_09681 | chr1:223926086-223926867 | CD14 | SE_23408 | chr1:223924747-223925696 | Colon_Crypt_1 | SE_23408 | chr1:223925806-223926930 | Colon_Crypt_1 | SE_24051 | chr1:223924902-223925357 | Colon_Crypt_2 | SE_24051 | chr1:223926231-223926878 | Colon_Crypt_2 | SE_25230 | chr1:223924752-223925398 | Colon_Crypt_3 | SE_25230 | chr1:223926296-223926903 | Colon_Crypt_3 | SE_26209 | chr1:223926103-223928290 | Duodenum_Smooth_Muscle | SE_26925 | chr1:223924658-223925356 | Esophagus | SE_26925 | chr1:223926095-223928145 | Esophagus | SE_31491 | chr1:223923671-223928232 | Gastric | SE_33950 | chr1:223925357-223926983 | HCC1954 | SE_34545 | chr1:223926186-223927072 | HCT-116 | SE_37129 | chr1:223924560-223926499 | HSMMtube | SE_37129 | chr1:223926584-223928521 | HSMMtube | SE_38254 | chr1:223923616-223925758 | HUVEC | SE_42269 | chr1:223923682-223925587 | Lung | SE_42269 | chr1:223925796-223927012 | Lung | SE_45872 | chr1:223924624-223925533 | Osteoblasts | SE_50365 | chr1:223924735-223925579 | Sigmoid_Colon | SE_50365 | chr1:223925795-223926977 | Sigmoid_Colon | SE_53249 | chr1:223926157-223926979 | Small_Intestine | SE_63671 | chr1:223924730-223925374 | HSMM | SE_64794 | chr1:223926064-223928210 | NHEK | SE_65644 | chr1:223924602-223925734 | Pancreatic_islets | SE_65644 | chr1:223925909-223927309 | Pancreatic_islets |
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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 |
GH01I223736 | chr1 | 223924574 | 223930136 |
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Enhancer Sequence | GGGCAGCTTA GGAACCTCCA GGCAGGGCCT CATCTGCTGC CGTTAGTAAT AAACATGGCC 60 AGCAACAGCC AGGGCCCTGC TAGCGGGAGA TGTCATCGGT AGCCACCTTC CTTCTCTGCA 120 GAGACACCGT CTGTCCCATG GATGAGCAGA GTCCCCTGGG GACCCAGCTC TGACACTTGT 180 CCTTGCTCAT GTCCAGGGTG CTGGACAGAC TGAGGCAGGT GTCAGGCTCC TGGGATGAGA 240 AAGGCAGATG AGAGATGGGA GTGGGAGCTT TACAGTGACT TAGGCAGAAT TGCTTAGTAT 300 TTACATATGC CTTACCTCAT TCCACAGAGA ATTTAAGGCC TGACCAAAAG AGACGGGGCG 360 GGGGGTGGGG GGGAGAGAAT ACAATAACAC CATGTACTGT AAAGAAAAAC AGTCAGTTCT 420 AAAAGAAAAA CAACCCAGAA AGAAGGGAAT GTGTCAAAAC CGGGAGAGGG GAAAAAAAAA 480 GGCATGCATG CTTTCAAAAG CACCTTAGGG GCTACAGATG GGCCCTATAC TTAGTGTTGA 540 CACCCAACAG CCATAAAAGA ATCTCACTGT GCCCCCAGGG GAGCACAGGG AAGGTCTGAT 600 TCTAGATTTT TTCTGTGCCA TTTATTTATC TATATCCTCA TGCACAAGTT CTATACTGTT 660 TTAATTGCTG TAGCTTTTTA TGTGTTTAAA CATCTAATAG AGGTAGACTT CCTTCTCTTA 720 GATTTTTTTC TAGCTATGCT TCATATTTAA TTTTTAAATA AACTTATCAG AATCAGCTAA 780 GTTCAAAAAC AATTTTTAAT CTTATTACCT TTTTTTTTCT TTTTTGTGAG ACGGGGTCTT 840 GTTCTGTCAC CCAGGCTGGA GTACAGTGGT ACAATCATAG CTCACTGCAG CCTTGACCTC 900 CCAGGTTCAA AGTGATTCTC CTGCCTCAGC CTCCCAAGTT GCTGGGACGA TAGAAGCATG 960 ACACCACACC TGGCTAATTT TTTAAAAATA ATTTTTATAG AGACAGGGTC TCACAGTATA 1020 GTGAGATTTC AGGGTGGTCT TGAAATCCTG AGGGCTCAAG AAATCCTCCA GCCCTGGCCT 1080 CCCAAGAGCT AGAATTACAG GCATGAGCCA CCGTACCTAG CCCTATTGCT ATTTTTATTA 1140 GCATTACATT AAGTTTATAG GCTAACTTAA GAGGACATGG CATTTTTATG ATAATGAGTT 1200 TTTGCAGTCA AGAACGCAGG CCAGTTTTTT TTAAATGGGG TAAATGATTG TCCAAGCGCC 1260 TCCAGGCAGG CTCACGTGCA CACTCTGGAG TCAGTGAAGA AGGTGAACAG CTGACAGGAG 1320 CAGCCTCCCA GTCAGAGAAG CCCTGCACAC TGTTGCAAAC AGACAGCTTG CATCTGGAGT 1380 CTTCTGTGAT CCGAGGAGGA AGCGTGGCTG AGTCCTTCCC AGAAGAGGGT CTGGAGCTGT 1440 GAGTTGGGGA CAATTGTCAG ATTCTAGCAG TGAAAGTGGT TCATGTGCAG GTGCAACCTG 1500 CCCCGCAGTC ACGGGACACA GCCACATGGA GCCGAGCCAC GCTCTCAGAG AAGGAGCCAG 1560 GGAAGAAACA CCCTAACTGC ACTCCTCCCT TCTTCTGGCC CCCAGCAGCC ATAGGCCCTG 1620 GGCCCCCGGT GAGATACCCA TAGAGATCAG CTCCCAGGCA GCAGGATGGA GGGTGTAGAC 1680 TGGACATGAA GAGGCAGCTG GAATGTATCG GGCACTCAGC TCCAGCTCAC CACGATCCAG 1740 GCACTCAAGT TCCCAAGACA ATAGTTTCTG CTCTCAGATA AATGGAATAA TTAAGGATCA 1800 AAAGGTTATC AACAGGTAAC CAAGCATAAA 1830
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