| Tag | Content |
|---|
EnhancerAtlas ID | HS136-19952 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr9:38046070-38048640 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GLI2 | MA0734.2 | chr9:38046525-38046540 | CATCTTGGGTGGTCA | - | 6.13 | | ZNF263 | MA0528.1 | chr9:38048102-38048123 | ACCTTCTCATCCCCCTCCTCA | - | 6.25 |
|
| | Number of super-enhancer constituents: 40 | ID | Coordinate | Tissue/cell |
| SE_00446 | chr9:38045747-38049347 | Adipose_Nuclei | | SE_01843 | chr9:38046152-38049346 | Aorta | | SE_02310 | chr9:38046305-38049227 | Astrocytes | | SE_04803 | chr9:38046770-38048376 | Brain_Cingulate_Gyrus | | SE_05785 | chr9:38046345-38048668 | Brain_Hippocampus_Middle | | SE_23246 | chr9:38046063-38049111 | Colon_Crypt_1 | | SE_24298 | chr9:38046291-38046575 | Colon_Crypt_2 | | SE_24298 | chr9:38046599-38048217 | Colon_Crypt_2 | | SE_24298 | chr9:38048224-38048921 | Colon_Crypt_2 | | SE_26555 | chr9:38045401-38049172 | Esophagus | | SE_27864 | chr9:38045888-38049329 | Fetal_Intestine | | SE_28791 | chr9:38045859-38049065 | Fetal_Intestine_Large | | SE_31580 | chr9:38045924-38049491 | Gastric | | SE_33929 | chr9:38045505-38049339 | HCC1954 | | SE_34811 | chr9:38045382-38049638 | HeLa | | SE_36884 | chr9:38046003-38048334 | HMEC | | SE_38030 | chr9:38045868-38049525 | HUVEC | | SE_38998 | chr9:38046222-38048950 | IMR90 | | SE_40993 | chr9:38046204-38048239 | Left_Ventricle | | SE_40993 | chr9:38048259-38049182 | Left_Ventricle | | SE_41666 | chr9:38046198-38048280 | LNCaP | | SE_42283 | chr9:38045806-38049314 | Lung | | SE_44329 | chr9:38046297-38049224 | NHDF-Ad | | SE_44779 | chr9:38046563-38049370 | NHLF | | SE_45758 | chr9:38045918-38049671 | Osteoblasts | | SE_47196 | chr9:38029911-38057164 | Panc1 | | SE_47459 | chr9:38046113-38048759 | Pancreas | | SE_48861 | chr9:38046201-38048278 | Right_Atrium | | SE_51847 | chr9:38046298-38048909 | Skeletal_Muscle_Myoblast | | SE_52833 | chr9:38045965-38049401 | Small_Intestine | | SE_55662 | chr9:38045991-38049449 | u87 | | SE_57367 | chr9:38046058-38048166 | VACO_503 | | SE_57367 | chr9:38048192-38049021 | VACO_503 | | SE_57926 | chr9:38046119-38048165 | VACO_9m | | SE_57926 | chr9:38048223-38048625 | VACO_9m | | SE_63571 | chr9:38046244-38049004 | HSMM | | SE_64986 | chr9:38046170-38049325 | NHEK | | SE_65279 | chr9:38044665-38046524 | Pancreatic_islets | | SE_67542 | chr9:38045991-38049449 | u87 | | SE_69063 | chr9:38047228-38048255 | 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 |
| GH09I038045 | chr9 | 38045447 | 38049805 |
|
Enhancer Sequence | AAAATTAGCC AGGCGTGGTG GTGTGTGCCT GTAATCCCAG CTATTCAGGA GGCTGAGGTG 60
GGAGAATCGC TCAAAACCGG GAGGCGGAAG TTGCAGTGAG CCGAGATAAG AAAAAAAAAG 120
AAAAGAGGCA CCTAATGTTT TCAGCCAGGG TTGGGCAAAG CTTCACTTCT GTAAGTAAAG 180
CATTGCTGAA CGTGGCCAGG CCTGCTCATT TATATATTGT CTGTGGCTCC CTGAAGAAGT 240
GAACAGAGGC AACAGAAACC GTGTTGCTGC AAAGCCTGAA ATACTATTTG GCCCTTTACA 300
GAAAAAGTTT GTGACCTCTG TGTTAGACAC ATAAGAATTG AATACAGGCA AACAAGAACA 360
AGCAGTTGCC CTGAGGGCAA TATACTGATG CTCGAAGCCC CCCCGGGTCC TCCTTCTCCG 420
AGTAGGGCCC TCAGGAGACA CCACATTCCT CTGAACATCT TGGGTGGTCA ATCTTCCATA 480
CTCTGGAGTG GATTTAATTT CTAGAAACTG CCCACGGCTT TTCCAAACCA ATTTAGGTGA 540
AAAGGTGGGT GATCACGCCA AGCAATGAAA CATACAAACT TGCCAGGGGC AGGACGCAAG 600
CCTCTAACAC GGAAGGAATT GAAATCGCAA TGAGATGTGG CTTCATTGTA AAGTTGCACA 660
ACTTGGTTTC TTGTGTCTCA TTAATTGGGG ACAACAGTCA TATAATGTTT GGGCCTCGGC 720
CTGACAGGCC TGACAGTAAA AATCCCTTCG TCGCTTGTGG CTTATGACTA CCTCTTACAA 780
GACAAACCAC ATTCCACAGG AACCTGCGGT CTGGAGAGGG CTGTTAAGGG CTGTCCTGGG 840
AAGTTTTTGG AAAAGATGGG GCCTGGTGAG AGAAAAGAAC ACCTGGCCTT TTTACAAATG 900
CAGACACTGT GGCCCAGGGA GGGGAGGGGC CTTGCCAACA TCACCTAGCC ATGGCACCTC 960
AAGGTTCAAC GTACCCAAAG TGGCCAGTGT TTCAGGTTCA GTGCCAGCTG TGGGGGATGA 1020
GTGAAAAATG AGTTCATGTT CTCCAAGAGT CCAGTCCCTG GTATCCAGAT AACACAGGAA 1080
TGTCAATAAA AACAGAGAAG TTTGGCAGGC CTTGGGTATG TCCCCTGACC TCTCCAAGTC 1140
TGCTTACTTG TATGAAAAAT AGTATCTTCC TTACACAATT CCTGTGAGGA CTCCAATGAG 1200
AGATGTACCT GAAGCACCCA GCAGAGTATA GCATACAGTA AGTGCTCAAC TGAAAGCAGC 1260
TAATCACTTC AGGCACAAGG CTGAGCTATT TTCTAGTTGC AGCGGTCCAA TCTTCTTACC 1320
CACAAGTGTG TACACACACC TCCCCTTCGG TGCAGAAAAC TGGAGACTGC AAGGCTTCAC 1380
TGAGCACCTG TCCTGTGTGA GGAATGGCCC TGCCTGCCTC CAACAGGGAA GTTAACAGAG 1440
GGGAAAACTG CAATCTGGCT CTGGAACTGC AACATTCCTA CCCCTCTTGG CTAATGCCTT 1500
CAGCAGGACC ACAATTATAA ACACAGAACT AACAGGAACT GAGAAACAGC AGCAGATCAA 1560
AAAGCAGGTT GCTCTTGCTT TTGGAGGATG TGAGACAGAT TTCTTCCAAA GAGGCAAGGG 1620
AAAATCCCCC ATCTTTACAG GTCAGGAATA GCGCCAGTAA ATCCCTCCAC TTTGTCCTTT 1680
CTCCTTTCAT GGAATAGCCC AATGCGCCAG TGGGTGTTAA GCAAACAAGG GTGTGAGTTG 1740
CAGCTTCCTG TGCCTGACTA TGCAGTTCCC GCACAGGTCC TTGCCCGAGC TAACGCTGTG 1800
GCCCCGGACA CAGACAGATA AAGTCCCGAT CGAACACTAA GGGCCAAAGC TGGCACCAAT 1860
GAGCAAGCCT GGTGAGCTTA TATAACAAAG GGCTTGTCAC CACTTCCTGT GATCCTCATC 1920
GCCAGCATTC CAACACAATG AGACACTCAG CGGCTTTGAA GTTCAACAAC TCATTCAGAT 1980
GGCCCCAGCA AAAACTCTGC TGGGAGGTGG AGAGCCTGTG CTCCCTTACC TCACCTTCTC 2040
ATCCCCCTCC TCACGTTGTG CTTGCAATGT TACCACTTCA AAAAAATTTC CAATAGTAAT 2100
TAAATGATTT GCATTTGTTT TTAAAAACTG TAAAATATTC CAACCTTCCA GCGATAACCA 2160
GTGTATACAT TTTGGTCGAT TTCCTTCCAG TCTTTTTTCT ACATATGTCG GTGGGAATGC 2220
AGTAATTGGA AAAGAATACA AATATTCATC ATTTTTTATA TCCTGCGTTT AAAAAAGTAT 2280
TACTTCTGGC CAGTTGCAGC AGCTCATGCC AGTAATCCTA GCACTTTGGG AACTGAGGTG 2340
GGAGGATCAC TTGAGTTTGA GATCAGCCTG GGCAGCACAG TGAGAGCCTG ACTCTACATA 2400
AAATTTTTAA ATTAGCTGGG CATGGTGGTG AGTGCCTGTA GTCCCAGCTA CGTGGGAGGC 2460
TGAGTCTGGA GGATCTCTTC AGCCCTTGAG GTGGAGGTTG CTGTGAGCTA TGATGGCACT 2520
GTTGCACTCT AGCCTGGGTG ACATAGCAAG GCCCTGCCTC AAAATAATAA 2570
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