Tag | Content |
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EnhancerAtlas ID | HS163-00020 |
Organism | Homo sapiens |
Tissue/cell | PrEC |
Coordinate | chr1:16499240-16501880 |
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 | Spz1 | MA0111.1 | chr1:16499568-16499579 | AGGGTATCAGC | + | 6.32 | TFAP4 | MA0691.1 | chr1:16501598-16501608 | ATCAGCTGTT | - | 6.02 | ZEB1 | MA0103.3 | chr1:16500289-16500300 | GGGCAGGTGGG | - | 6.14 |
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| Number of super-enhancer constituents: 26 | ID | Coordinate | Tissue/cell |
SE_23091 | chr1:16499347-16501823 | Colon_Crypt_1 | 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 | chr1:16499336-16504399 | 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 | chr1:16499250-16512083 | Panc1 | SE_47539 | chr1:16499523-16500148 | Pancreas | SE_47539 | chr1:16500355-16501118 | Pancreas | SE_47539 | chr1:16501350-16501756 | Pancreas | SE_48744 | chr1:16501448-16503785 | Right_Atrium | SE_50427 | chr1:16497958-16504232 | Sigmoid_Colon | SE_52536 | chr1:16497970-16501408 | Small_Intestine | 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 | GAGATCGAGA GCAGCCTAGC CAACATGGTG AAACCCCGTC TCTACTAAAA ACACAAAAAT 60 TAGCTGGACG TGGTGGTGGG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA 120 ATTGCTGGAA CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG ATCACGCCAT TGCACTCCAG 180 CTGGGGCCAA CAACAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AGAAAAAGGA 240 ATCTGAGCAT GGAGGCACCC TCCACCTTCG GATTGCTAGG AGATCAATGT CTGGCCCCGA 300 GTGGGTGAGG CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA GTTCACGGGG 360 CCTCTTCCTC TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG CAGGAGTCCA 420 GGCTCATAGA GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA CCATTCCCAC 480 TGGGGCATAC AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT TTTGCGGAAG 540 AACTAACCAC ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG TGAGTCAGTT 600 TTATTATATG AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC ACACAGACAG 660 TGCTCAGCGA AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT CCCCAGCTTC 720 TCTGGGGGAT CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC ACTACTCCCA 780 GCCTTTGTCC CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT GGAGCTTCCT 840 CCTCTGGTCC TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG TGCCAGAGCT 900 GCCCAGCCTG CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG CCCAGGCCTC 960 GGGCAAACAG AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC ATTCCTGGGG 1020 GGTGCCGTGG CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG ACACCTGCCT 1080 CTGTTACCTT GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC CTGGGGCAGG 1140 GGGATGGAGT GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT TGAACAAGGC 1200 CTCTCTGAGC CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT AGCCTTCTGG 1260 TGGGCTTATG GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA TCAGCCTGCC 1320 TCACCGTGAG GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG GGGGTCTTCT 1380 GGCTCTGGGC CCTAGAATGG GGCTGAAGCC CAGAGAGGCA GTTGCACCTC CCCTAGGCCA 1440 CACAGCAGGT ATAGGCCCCA GGGGCTGAGT GCCCATCATG CCTGCCCTCC TCTCCATCCA 1500 CCCAGAGCCT CACTAGCCAG ACCCGCACTC TCCCATCCCC TGGGCAAGTC TGCACCCCAG 1560 GTCGGTGAGG ACTCCCAGAT TCTACTCCCA CCAGCCAGGG CCAGACCTGG TGCAGGAGGC 1620 TCCACAGTTC TCCTGCTCGG GGCTCCGTCT CCCCACTTCC TGGAGCTCCA TCCAAGTGGG 1680 GAACCCTGCC CGTCCTCTGC CCCTCAAGCC AACCAGGCAT TTACGGGGGA TGGGGCAGGG 1740 AGGGAGGCCA GGACCTGCAT CCTTCCAGCC CTGGCCCTCA GCAACCCCAT CAGGCAGTCA 1800 GGGGAGGAGC CTCCCCCAGG GAATCCTCCC TCCCTCTGTG TTGGCCTGGC CAGGTTCTCC 1860 TCTCTCTGTC TGCCTTTGTC TTTTTCTCTC TGTCTCTTCA TCCCAGGAAG AGGCCACAGG 1920 ACAGGGGTGT CCCAAGCACA GAAGAAACTT GTCTGATGAA AACAGGCCTT GGCTGGGAGC 1980 AGGGCCATCT GGATTTGCAC CCTGATTCTG TCTGACTTGC TGTGTGACCT TGGGCGAGTC 2040 CCCTCCCCTC TCTGGTCTTT CCCATTATTA TCTACCCAGC ACATAGTAGG TTCTCGGAAA 2100 AGGGGAGTCA CATATGCGTG CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT TTAATCCCCA 2160 CAGATCTGCC AGCCTTTGAT ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG AATAGGAAGC 2220 TGAGGGCTCA TGGGCTGCGG GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC CTGCCCGAGG 2280 GAGGGGGCTG TGGGCCCCTC GCCATTCACT GCTAAGCCTG GATCCGGGCG CCTTTGTGCC 2340 AAGAACAAAA CCCGGGGGAT CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT CCGGAAGGGA 2400 CGGAAGCCTG GGCCTGAGGG GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC 2460 TGGCCCCATA CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA 2520 AACCTGGGTT CAGATCCCAC CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC 2580 TCGGAGCCTC AGTTTCATGA TCTGTAAAGT GGACATTAGA GTCGCTCGGG ATGCGGGATG 2640
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