Tag | Content |
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EnhancerAtlas ID | HS098-00583 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr1:16498570-16500640 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | - | 7.07 | MAFF | MA0495.3 | chr1:16500147-16500162 | CTGCTGACTCAGCGC | + | 7 | RREB1 | MA0073.1 | chr1:16498769-16498789 | CCCCCTCCCACCCCACCCCA | + | 6.5 | Spz1 | MA0111.1 | chr1:16499568-16499579 | AGGGTATCAGC | + | 6.32 | ZEB1 | MA0103.3 | chr1:16500289-16500300 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 29 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16497584-16499266 | Colon_Crypt_1 | SE_23091 | chr1:16499347-16501823 | Colon_Crypt_1 | SE_23751 | chr1:16497995-16499231 | Colon_Crypt_2 | SE_23751 | chr1:16499364-16501671 | Colon_Crypt_2 | SE_24743 | chr1:16497841-16502803 | Colon_Crypt_3 | SE_26540 | chr1:16496436-16504779 | Esophagus | SE_28102 | chr1:16497879-16504574 | Fetal_Intestine | SE_29455 | chr1:16497964-16506131 | Fetal_Intestine_Large | SE_31527 | chr1:16497806-16499321 | Gastric | SE_31527 | chr1:16499336-16504399 | Gastric | SE_34268 | chr1:16497740-16504248 | HCT-116 | SE_34628 | chr1:16497415-16506115 | HeLa | SE_36144 | chr1:16498765-16501519 | HMEC | SE_38062 | chr1:16499064-16503878 | HUVEC | SE_44998 | chr1:16499693-16500212 | NHLF | SE_46140 | chr1:16499323-16500582 | Osteoblasts | SE_47150 | chr1:16497663-16499232 | Panc1 | SE_47150 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16499523-16500148 | Pancreas | SE_47539 | chr1:16500355-16501118 | Pancreas | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16497970-16501408 | Small_Intestine | SE_56795 | chr1:16496450-16499306 | VACO_400 | SE_56795 | chr1:16499345-16504738 | VACO_400 | SE_57357 | chr1:16499350-16500174 | VACO_503 | SE_57357 | chr1:16500236-16501136 | VACO_503 | SE_57939 | chr1:16499369-16500862 | VACO_9m | SE_64726 | chr1:16499137-16501292 | NHEK | SE_65472 | chr1:16498579-16501949 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 16499607 | 16500371 | chr1 | 16499761 | 16499895 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I016171 | chr1 | 16497941 | 16511884 |
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Enhancer Sequence | ATGTCTCCGA GGGAGGGGCA TTAGCACAAC AGACACTGCC TCTCAGCCCC GAGTCCCCAG 60 ATCCATGTCA TCTATTGGAG TCTCCCCCAC TGTAAACCTG CAAGGGCAGC CACGGCCGGG 120 AGCAGCTGGT CCTGAGACTT GGGCAGAGGC CCTGGACAGT GGGGCAGAAG CGCTTGGCTG 180 GCCAGGAATT GGATCACTGC CCCCTCCCAC CCCACCCCAT TCAGCCCTGT CTCCCACGGA 240 CTCTGACCAC CCCTTGGTTC TCTTATCAAA AACCGCCAAA ACCCGCCATC GAAACTCCCA 300 GCCTCCTGAC CCCCATGCCC CACCCGGCTC CACCCGTCTT CCCAACCTGG CATCCAGTGC 360 CCCAAACCTG CCTATTCCGT TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT GGCACCAGGA 420 GGCCAACAAC CCAGGCCCCC TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC CTCCACCCTA 480 CTGTTTCTCC TGGGGTGTGC CTTTCTTTGC CTTATGCCTC GGCATCTCTA AGTGGCAGGG 540 GATGGAGTGG AGTGAGGGCG GCAGGCCAAG GGCATGGCCC ATAATGAAAA AGGAATCTGG 600 TTGGGCATGG TGGCTCACCC TTGTAATCTC AGCACTTTGG GAGGCCAAGG CAGGCAGATC 660 ATGAGGTCAG GAGATCGAGA GCAGCCTAGC CAACATGGTG AAACCCCGTC TCTACTAAAA 720 ACACAAAAAT TAGCTGGACG TGGTGGTGGG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG 780 AGGCAGGAGA ATTGCTGGAA CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG ATCACGCCAT 840 TGCACTCCAG CTGGGGCCAA CAACAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA 900 AGAAAAAGGA ATCTGAGCAT GGAGGCACCC TCCACCTTCG GATTGCTAGG AGATCAATGT 960 CTGGCCCCGA GTGGGTGAGG CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA 1020 GTTCACGGGG CCTCTTCCTC TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG 1080 CAGGAGTCCA GGCTCATAGA GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA 1140 CCATTCCCAC TGGGGCATAC AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT 1200 TTTGCGGAAG AACTAACCAC ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG 1260 TGAGTCAGTT TTATTATATG AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC 1320 ACACAGACAG TGCTCAGCGA AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT 1380 CCCCAGCTTC TCTGGGGGAT CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC 1440 ACTACTCCCA GCCTTTGTCC CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT 1500 GGAGCTTCCT CCTCTGGTCC TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG 1560 TGCCAGAGCT GCCCAGCCTG CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG 1620 CCCAGGCCTC GGGCAAACAG AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC 1680 ATTCCTGGGG GGTGCCGTGG CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG 1740 ACACCTGCCT CTGTTACCTT GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC 1800 CTGGGGCAGG GGGATGGAGT GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT 1860 TGAACAAGGC CTCTCTGAGC CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT 1920 AGCCTTCTGG TGGGCTTATG GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA 1980 TCAGCCTGCC TCACCGTGAG GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG 2040 GGGGTCTTCT GGCTCTGGGC CCTAGAATGG 2070
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