| Tag | Content |
|---|
EnhancerAtlas ID | HS039-00700 |
Organism | Homo sapiens |
Tissue/cell | ESC_NPC |
Coordinate | chr1:205268490-205271190 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr1:205268583-205268595 | AAACAAACAAAC | - | 6.32 | | ZNF263 | MA0528.1 | chr1:205270899-205270920 | GGAGGAGAAGGAGGCAGGTGG | + | 6.06 | | ZNF263 | MA0528.1 | chr1:205270905-205270926 | GAAGGAGGCAGGTGGTGGGGG | + | 6.12 | | ZNF263 | MA0528.1 | chr1:205270887-205270908 | GGAGCAGGGGTGGGAGGAGAA | + | 7.6 |
|
| | Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
| SE_02431 | chr1:205266405-205271883 | Astrocytes | | SE_05801 | chr1:205270061-205271793 | Brain_Hippocampus_Middle | | SE_11085 | chr1:205269398-205291943 | CD20 | | SE_29391 | chr1:205269640-205272065 | Fetal_Intestine_Large | | SE_32765 | chr1:205268836-205269840 | H1 | | SE_32765 | chr1:205269866-205270789 | H1 | | SE_32765 | chr1:205270884-205273251 | H1 | | SE_38936 | chr1:205268676-205271834 | IMR90 | | SE_41963 | chr1:205270131-205271083 | LNCaP | | SE_46173 | chr1:205266256-205272586 | Osteoblasts | | SE_47803 | chr1:205269912-205271336 | Pancreas | | SE_50327 | chr1:205270013-205271836 | Sigmoid_Colon | | SE_52983 | chr1:205270102-205271453 | Small_Intestine | | SE_54130 | chr1:205269862-205271873 | Spleen | | SE_56704 | chr1:205269883-205271754 | u87 | | SE_56879 | chr1:205269902-205271377 | VACO_400 | | SE_58462 | chr1:205242169-205295027 | Ly1 | | SE_58967 | chr1:205242236-205295022 | Ly3 | | SE_60263 | chr1:205242326-205284722 | Ly4 | | SE_60576 | chr1:205242267-205294889 | DHL6 | | SE_61365 | chr1:205242037-205294994 | HBL1 | | SE_61423 | chr1:205183427-205322469 | Toledo | | SE_62465 | chr1:205242393-205294944 | Tonsil | | SE_65493 | chr1:205266941-205268842 | Pancreatic_islets | | SE_65493 | chr1:205269316-205274025 | Pancreatic_islets | | SE_68815 | chr1:205268850-205274019 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I205293 | chr1 | 205262232 | 205274585 |
|
Enhancer Sequence | AATTGCGTGA GCCCGGGAGG CGGAGCTTGC AGTGAGCCGA GATCACACCA CTGCACTCCA 60
GCCTGGGTGA CAGAGCGAGA CTCTGTCTCA AAAAAACAAA CAAACAAAAA AACACTCTTC 120
TGCTTCTCCC ACTCACTCTC TCTCTCTCTC TCTTTTTTTT TTTTTTTTTT TTTTTGAGAC 180
TGAGTCTTGC TGTCACCCAG GCTGGAGTGC AGTGGCGCAG TCTAGGCTCA CTGCAACCTC 240
TGCCTCCCGG GTTCAAGCAA TTCTCCTGCC TCAGGCTCCC AAGCAGCTGG GACTACAAAC 300
ATGCTCCACC ATGCCTGGCT AATTTTTTTT GTATTTTTAG TAGAGACGAG GTTTCACCAT 360
GTTGGCCAGG CTGGTCTCGA ACTCCTGACC TCAGGTGATC CATCCACCTT GGCCTCCCAA 420
AGTGCTGGGA TTACAGGCAT GAGCCACCAC GCCTGGCCTC ACTCTCTTCT TTCTTAGCTT 480
TCTCTTGGGG CTTGTGGAGA CTAGGAAAGG GCACTTGGGA AATTGGCATA TTCCTTGTGC 540
CTGCAAAAGA ACCTGGCATA TAATGGATGC TCATATAATA AATATTTATA AATAAACCTG 600
GCATATAAAT TTATAGTTCC TTCACTTACA TTCTTTTATC CAATTCTCCA AACACCATGC 660
CATTCAAGTG AGTCTGTGGG ATGCCAAACC TGGGTTTGAG GTCTGATTTC TCCATTTGCT 720
ATCAAGTTCC TTTTTTTTGA GACAGAGTCT TGTTCTGTTG CCCAGGCTGG AGTGCAGTGG 780
CACAATCTCA GCTCACTGCA ACTATCGCCT CCCAGGTTCA AGGGATTTTC CTGCCTCAGC 840
CTCCCGAGTA GCTGGGCCTA GAGGAGTGCG CCACCATGAC CGGCTAATTT TTTGTATTTT 900
TAGTAAAGTC AGGATTTCAC CATGTTGGCC AGGCTGGTCT CGAGCTCCTG ACAAGTGATG 960
CTTCTGCCTC GACCTCCCAA AGTGCTGGGA TTACAGATGT GAGCCACTGC GCCTGGCCTA 1020
CTTAATGTTT TTGAGTCTCC ATTTCTTTTA TAAAATGAGA ATGATAGAAA TAGTACTGAA 1080
CTAACAAGAC TATCGTGAGC ATTACATGAG GTAACACACC TAAAGGGCTT GACCCATAAG 1140
CACTTAGTGA ATGGTAGCCC CTATTATTAT CTCCGAAGAT GCAATTCTTT CCATCATCCA 1200
AACTCCCTTT TTCTTCTTTT TTTTTTTTTT TGAGACCAGG CTGGAGTGCA GTGGTGCGAT 1260
CTCTGCTCAC TGCAAGCTCC GCCTCCTGGG TTCACGCCAT TCTCCTGCCT CAGCCTCCTG 1320
AGTAGCTGGG ACTACAGGCG CCCGCCCCCG CGCCCGGCTA ATTTTTTATA TTTTTAGTAA 1380
AGACGGGGTT TCACCGTGTT AGCCGTGATG GTCTCGATCT CCTGACCTTG TGATCCGCCC 1440
ACCTCTGCCT CCCAAAGTTC TGGGATTACA GGCATGAGCC ACCGCGCCGT CCCCAAACTC 1500
CCTTTCAACA TGATCTGAAC CAATAACAAT TTCTCACTGA ATTGCATGCT ACCTTACCCA 1560
CAGCCTGTAA CCTCCTTGAG GCTAAGATCT CTGTTTTTTT TTTTTTTTTT TTTGCACCAG 1620
GGATACAGCA ATTACCTCTG TCTTCTACTA AGCTTAGCAC ACAAAAGGGC TTGATTCATG 1680
AGAGGAATGA ATAAAGGAGC ACTGCTACCC CCACAGCTGA ACTCTAAGCT TCTGGAGATA 1740
AACCCACCCC CTGGATTTTT TCCATGTTTA CCCAGAGTCT AGCCCAGAGT TCCAGCACTG 1800
AGTAGGACCT CAGAGACTTA AGACCTAAGT ACTCCAGTGT CGCCTAAGCA ATGTCTTGTT 1860
TGCTCTCCCA TCTTGACCTC ATAGTTGCCT TGCCCTCCCC ATCTCCTTTG CAGACTAGTG 1920
ACTTTGCCAG CTCAGCTCTC CAGGTGTGGG AGGGGAGGTC CAACGCGCTC CACTGGGCAG 1980
GCACCGACAG CCGGCAGGAC AGGTGTGTTG TGGGGCCAGA GCCAGAGCTG GGGACGTTTG 2040
GAGGCCTCCT GTGACTACCA GAGTGGGTCG GGGTGGGGGA GGGAGGCTGC CTGAAGCCAG 2100
AGCCAGCCGG CTGCTGGCCG GCACTTTGTC CTCATCCTCC CTTTCATCCC CAGCCCTCGG 2160
AGCCTGGGAG TTTCTCAATG GAGCAGGCGT GTGGGGAATG CTCTGCAGGG GGCTGAGGGA 2220
GTTGGCGTAC GGTGGGGGTG GACATTCCAG GCATTCTTTG CTTTCTCTGG GAGTCAGGCA 2280
GTGAGGACGG AGGGGGGAAA AGCTGCCCAG CACCAGAGTA AAGGGGATTT CTTAGGAGGG 2340
AGAGAATAAA GGCTGTGGGG GTGTCTTTAC GCAGCAGGAG CAGGGCTCAA GCAGACAGGA 2400
GCAGGGGTGG GAGGAGAAGG AGGCAGGTGG TGGGGGCAGG GTGGGATAAT CTGCCAAATC 2460
CACTTCTACT TTAGTGCCAA AGGCCGGAAG AGCAACTGGG ACCCTGGGCC CAGGGCCTTC 2520
CCACCTGTGT GCTTAATAGG GTCAGGCCAG AGCTACTGAG CTCACGTTTG TTTTGATTCG 2580
GCAGTTTTTC TATTTCCCAT CCCTGGCAGC CTAGGGGAAC GAGTATTAGG AGAAGGCTCA 2640
AAAACCTGCT CAGCACCATC CCTCCCCACC TCAGTCACCA AAGAGAACAG CAGGGCCTGC 2700
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