| Tag | Content |
|---|
EnhancerAtlas ID | HS176-41583 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr9:38046350-38048850 |
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: 38 | 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 | chr9:38046599-38048217 | 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_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 | ATACTATTTG GCCCTTTACA GAAAAAGTTT GTGACCTCTG TGTTAGACAC ATAAGAATTG 60
AATACAGGCA AACAAGAACA AGCAGTTGCC CTGAGGGCAA TATACTGATG CTCGAAGCCC 120
CCCCGGGTCC TCCTTCTCCG AGTAGGGCCC TCAGGAGACA CCACATTCCT CTGAACATCT 180
TGGGTGGTCA ATCTTCCATA CTCTGGAGTG GATTTAATTT CTAGAAACTG CCCACGGCTT 240
TTCCAAACCA ATTTAGGTGA AAAGGTGGGT GATCACGCCA AGCAATGAAA CATACAAACT 300
TGCCAGGGGC AGGACGCAAG CCTCTAACAC GGAAGGAATT GAAATCGCAA TGAGATGTGG 360
CTTCATTGTA AAGTTGCACA ACTTGGTTTC TTGTGTCTCA TTAATTGGGG ACAACAGTCA 420
TATAATGTTT GGGCCTCGGC CTGACAGGCC TGACAGTAAA AATCCCTTCG TCGCTTGTGG 480
CTTATGACTA CCTCTTACAA GACAAACCAC ATTCCACAGG AACCTGCGGT CTGGAGAGGG 540
CTGTTAAGGG CTGTCCTGGG AAGTTTTTGG AAAAGATGGG GCCTGGTGAG AGAAAAGAAC 600
ACCTGGCCTT TTTACAAATG CAGACACTGT GGCCCAGGGA GGGGAGGGGC CTTGCCAACA 660
TCACCTAGCC ATGGCACCTC AAGGTTCAAC GTACCCAAAG TGGCCAGTGT TTCAGGTTCA 720
GTGCCAGCTG TGGGGGATGA GTGAAAAATG AGTTCATGTT CTCCAAGAGT CCAGTCCCTG 780
GTATCCAGAT AACACAGGAA TGTCAATAAA AACAGAGAAG TTTGGCAGGC CTTGGGTATG 840
TCCCCTGACC TCTCCAAGTC TGCTTACTTG TATGAAAAAT AGTATCTTCC TTACACAATT 900
CCTGTGAGGA CTCCAATGAG AGATGTACCT GAAGCACCCA GCAGAGTATA GCATACAGTA 960
AGTGCTCAAC TGAAAGCAGC TAATCACTTC AGGCACAAGG CTGAGCTATT TTCTAGTTGC 1020
AGCGGTCCAA TCTTCTTACC CACAAGTGTG TACACACACC TCCCCTTCGG TGCAGAAAAC 1080
TGGAGACTGC AAGGCTTCAC TGAGCACCTG TCCTGTGTGA GGAATGGCCC TGCCTGCCTC 1140
CAACAGGGAA GTTAACAGAG GGGAAAACTG CAATCTGGCT CTGGAACTGC AACATTCCTA 1200
CCCCTCTTGG CTAATGCCTT CAGCAGGACC ACAATTATAA ACACAGAACT AACAGGAACT 1260
GAGAAACAGC AGCAGATCAA AAAGCAGGTT GCTCTTGCTT TTGGAGGATG TGAGACAGAT 1320
TTCTTCCAAA GAGGCAAGGG AAAATCCCCC ATCTTTACAG GTCAGGAATA GCGCCAGTAA 1380
ATCCCTCCAC TTTGTCCTTT CTCCTTTCAT GGAATAGCCC AATGCGCCAG TGGGTGTTAA 1440
GCAAACAAGG GTGTGAGTTG CAGCTTCCTG TGCCTGACTA TGCAGTTCCC GCACAGGTCC 1500
TTGCCCGAGC TAACGCTGTG GCCCCGGACA CAGACAGATA AAGTCCCGAT CGAACACTAA 1560
GGGCCAAAGC TGGCACCAAT GAGCAAGCCT GGTGAGCTTA TATAACAAAG GGCTTGTCAC 1620
CACTTCCTGT GATCCTCATC GCCAGCATTC CAACACAATG AGACACTCAG CGGCTTTGAA 1680
GTTCAACAAC TCATTCAGAT GGCCCCAGCA AAAACTCTGC TGGGAGGTGG AGAGCCTGTG 1740
CTCCCTTACC TCACCTTCTC ATCCCCCTCC TCACGTTGTG CTTGCAATGT TACCACTTCA 1800
AAAAAATTTC CAATAGTAAT TAAATGATTT GCATTTGTTT TTAAAAACTG TAAAATATTC 1860
CAACCTTCCA GCGATAACCA GTGTATACAT TTTGGTCGAT TTCCTTCCAG TCTTTTTTCT 1920
ACATATGTCG GTGGGAATGC AGTAATTGGA AAAGAATACA AATATTCATC ATTTTTTATA 1980
TCCTGCGTTT AAAAAAGTAT TACTTCTGGC CAGTTGCAGC AGCTCATGCC AGTAATCCTA 2040
GCACTTTGGG AACTGAGGTG GGAGGATCAC TTGAGTTTGA GATCAGCCTG GGCAGCACAG 2100
TGAGAGCCTG ACTCTACATA AAATTTTTAA ATTAGCTGGG CATGGTGGTG AGTGCCTGTA 2160
GTCCCAGCTA CGTGGGAGGC TGAGTCTGGA GGATCTCTTC AGCCCTTGAG GTGGAGGTTG 2220
CTGTGAGCTA TGATGGCACT GTTGCACTCT AGCCTGGGTG ACATAGCAAG GCCCTGCCTC 2280
AAAATAATAA TGATAAATAC ACATACAAAA AATGAAAAAG TATTACATTG TTGAGTGTTT 2340
TCCATCTTAA CGATATTGCA GTGGAGTTAC TCAACTCAGC TTTTGTTGGC TGTATTCCCT 2400
CTCACTTTAG GCCACACGTT AGCCACTTCC CATGGCTGGA TATTTAGGTA ATTTCCAGTT 2460
TTTGGTTTTG CCAAATGTTT TAGGTGCTTT TCCCTAGGAG 2500
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