Tag | Content |
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EnhancerAtlas ID | HS176-38144 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr7:104611800-104613660 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2C | MA0497.1 | chr7:104611802-104611817 | ATTTTAAAAATAGCA | + | 6.41 | ZNF263 | MA0528.1 | chr7:104613622-104613643 | AGAGGAGAGGAGGAGAGGGGA | + | 6.19 | ZNF263 | MA0528.1 | chr7:104613637-104613658 | AGGGGAGGGGAGGGGAGAGGA | + | 7.1 | ZNF263 | MA0528.1 | chr7:104613627-104613648 | AGAGGAGGAGAGGGGAGGGGA | + | 7.95 | ZNF263 | MA0528.1 | chr7:104613630-104613651 | GGAGGAGAGGGGAGGGGAGGG | + | 8.37 |
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| Number of super-enhancer constituents: 24 | ID | Coordinate | Tissue/cell |
SE_00068 | chr7:104613167-104615624 | Adipose_Nuclei | SE_02797 | chr7:104612072-104613635 | Astrocytes | SE_10864 | chr7:104613467-104615625 | CD20 | SE_23243 | chr7:104612195-104613684 | Colon_Crypt_1 | SE_23896 | chr7:104612206-104612833 | Colon_Crypt_2 | SE_23896 | chr7:104612854-104613156 | Colon_Crypt_2 | SE_23896 | chr7:104613167-104613408 | Colon_Crypt_2 | SE_23896 | chr7:104613455-104613673 | Colon_Crypt_2 | SE_25883 | chr7:104611348-104612482 | Duodenum_Smooth_Muscle | SE_27138 | chr7:104612115-104613557 | Esophagus | SE_31758 | chr7:104612157-104613520 | Gastric | SE_36016 | chr7:104611271-104615352 | HMEC | SE_40784 | chr7:104612124-104612879 | Left_Ventricle | SE_42639 | chr7:104612148-104613647 | Lung | SE_44335 | chr7:104611496-104615309 | NHDF-Ad | SE_44865 | chr7:104611959-104613661 | NHLF | SE_45643 | chr7:104611530-104615561 | Osteoblasts | SE_49374 | chr7:104612160-104613301 | Right_Atrium | SE_50161 | chr7:104612049-104615321 | Sigmoid_Colon | SE_52521 | chr7:104612007-104612844 | Small_Intestine | SE_54878 | chr7:104611624-104613271 | Stomach_Smooth_Muscle | SE_56051 | chr7:104611806-104615352 | u87 | SE_64615 | chr7:104611620-104615365 | NHEK | SE_67958 | chr7:104611806-104615352 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr7 | 104611802 | 104611909 | chr7 | 104612099 | 104612756 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I104970 | chr7 | 104611067 | 104615323 |
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Enhancer Sequence | TTATTTTAAA AATAGCATAT TGTAAAGGAG ATAATCCTAG ATTGTGTGGG TATAGTGTGT 60 GCATTTCTAT ATGTACATAG CAGTCATAAA GTAATATTCT GGGCACCACA AATCTAAAAA 120 ACGTCCAAGT CATGGAATCA TAGTAGAGAT GTCAAAGGGA GGGAAAGGGT GAGAAAAGGG 180 TGAACTGAAA AAACCTGATA GTATTATTTC TTCCTGCTCA GGGTTAATAA TATAGTAAAA 240 AGAGATTTTT ATTACATACA ACTAGAAAGG ACCAATTAGA GTGTGGAAAG TGTTCCTTTG 300 CATAGTCAAA TGATAGGCAG GGGAATATAA TTTCACCAGA AATTACTATA GCGAGTTTCA 360 ATAAAGGACT GCAGAACAAT AAGGCCTTGT TAATCCCATA CTGGTCTGTT CAAATAGTGT 420 GTAATTCAAA GCAATTGCTG CTCCCTAGGC AGGAATTTAC AATTGCTACA TGTGAAGGGA 480 GGATAATGTG TCATTCCAAG GGGAAATCAG GTTCTGGAAA GGGCCTCCTG GCTGCAGAAC 540 TGTATGTGTC CCCAAACAGC TCCACAGCAG GCCAAGTTAA ACAAAATAAG TAGAGAACCA 600 CCCTGTGAAA TGAGTCTGCT TCGAATTGAT CTGTATTTGC CTTGCTCTCT CCTGCCTTTT 660 TGGTGGATGA CAAAATGTCC CCAAACCAAG GATCAAGAGG GGAAGGCAGA GAAACTCAGA 720 CCTGAATAAG CTATCACTTA GAAATTGACT GCCTCCACCA GTGCACGGTG GCTCACGCCT 780 GTAATCCCAG CACTTTGGGA GGCCAATGCA GGCAGATCAC TTGAGCTCAG GAGGTAGAGA 840 CAGCCTGGGC AACATGGTGA AACCCCATTT CTAAAAAAAA TGCAAAAATT AGCTGGGCCT 900 GCTGGCACAT GTCTGTAGTC CCAACTACTT GAGGAGTGCT GAGACAGGAG AATTGTTTGA 960 GCCCAGGAGG TTGAGGCTGC AGTGAGCCAT GTTCATACCA CTGCACTTCA GCCTGAGTGA 1020 CAAAGTGAGA CCCTGTCTTA AAAAAAAAAA AAAAAAAAAA GGCAAGAAAA AGAAAAAGAC 1080 AGAAAAAAGA AAGTGACTCC TCCCACCCTA CTCCCCTACT TGGCAAGGGC ATACAACTTC 1140 ATTCAAGTGA ACTGCAGCCT ACATGTACGG ACTGTATGTA TATTTAATTG ATAATAGTGA 1200 TGCATACAGA GCACCATCCC TGGGCATAGA AACACTGGAC AAGAGTCAAA CATGAGTCAA 1260 CTGTAAGAGG AGGCTTGAAT CGTAATACAT TTTGAACAAT TATGGTCAAT AATCCTTCAG 1320 AGAACAACCC TTCAGTTCTA CGTTGTCATT TTTGTGGAAT TAAATGTGAA CAGCTTAAAA 1380 TTCCATACTG TTTTAAAACT CAGCTTTGAA TTCCAATGAC TGACTAATCC ATGCTCCCAG 1440 GGACACCAAG CTATGTCAGT CCTCCAACAA CATATTGTGA GGCCACGCTG AGCTGCTAAT 1500 TCCTGTGGAC TAGCTAATTA GGTAAAAAAT TAAATTAAAA ACGAAAAGCC CAGGCATGGT 1560 GGCTCATGCC TGTAATCCTA GCAGTTTGGG AGGCTTAGGC AGGAGGATTG CTTGAGCCTA 1620 GGAGTTTGAG ACCAGCCTGA GCAACAAAGT GAGCCCCTGT CTATACAAAA AAATAAAAAA 1680 TTTAAAAAAA AATTAGCATG GTGGCACACA CCTGTGGTCT GAGCTACATG GGAGGCTGAG 1740 GCAGGAGTAT TGCCTGAGCC TAGGAATTGA GGCTGCAGTG AGCTGTGTTT GTGCCACTGC 1800 ACTCCAGCCT GGACAACAGA GGAGAGGAGA GGAGGAGAGG GGAGGGGAGG GGAGAGGAGG 1860
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