Tag | Content |
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EnhancerAtlas ID | HS081-00114 |
Organism | Homo sapiens |
Tissue/cell | HACAT |
Coordinate | chr1:16499380-16501820 |
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 | GGAGGTTGCA GTGAGCCAGG ATCACGCCAT TGCACTCCAG CTGGGGCCAA CAACAGCAAG 60 ACTCCATCTC AAAAAAAAAA AAAAAAAAAA AGAAAAAGGA ATCTGAGCAT GGAGGCACCC 120 TCCACCTTCG GATTGCTAGG AGATCAATGT CTGGCCCCGA GTGGGTGAGG CCAGCCGAGG 180 TCACTTGAAG GGTATCAGCC CTGAGGAGGA GTTCACGGGG CCTCTTCCTC TCGGCCAACC 240 CCAGCAGAGC TTGGAAACTG AGGCCCAGAG CAGGAGTCCA GGCTCATAGA GCCGGCCTGG 300 CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA CCATTCCCAC TGGGGCATAC AGCGCCTTTC 360 TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT TTTGCGGAAG AACTAACCAC ACCTCAGGTT 420 CCCCTTATGA AAGACAGAGG CTGAGGAGAG TGAGTCAGTT TTATTATATG AGATAAGGCG 480 GCTGGACAAA GCAGCGACAC AGGGACTGGC ACACAGACAG TGCTCAGCGA AGCAGTCGCC 540 TTCCTTCAGG TCTGAAATCC TCACTCAGCT CCCCAGCTTC TCTGGGGGAT CTCCCTTCCC 600 CTCTCTGGAC CCCTGGGCCT GACTTCCCCC ACTACTCCCA GCCTTTGTCC CACTCCTGCC 660 CCAGGCACCC CTCCCTCCTT CATGGGAAAT GGAGCTTCCT CCTCTGGTCC TGCCACCACC 720 TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG TGCCAGAGCT GCCCAGCCTG CTGACTCAGC 780 GCCTGGGGAT AGGGCTTGCT TTAGGAACAG CCCAGGCCTC GGGCAAACAG AGCCACGGCA 840 ACCACACCCC TGCCACAGGA ATGCAGCAAC ATTCCTGGGG GGTGCCGTGG CACCGTGCCT 900 GTGACTGGGG GGCAGGTGGG GGGCAGGTAG ACACCTGCCT CTGTTACCTT GCCACAGGTA 960 GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC CTGGGGCAGG GGGATGGAGT GAGGTCATGA 1020 GGCTTTGAAA TCTGTACCAG CCATGTGACT TGAACAAGGC CTCTCTGAGC CTCAGTTTCC 1080 TCACCTGTAA GGTGAAGGGA GAATAGCGGT AGCCTTCTGG TGGGCTTATG GGGAGGACTG 1140 AACGAGAGTG CGCCCGTCTG GGGCTCAGCA TCAGCCTGCC TCACCGTGAG GATTCCGTGA 1200 AGCAGACCCT CACCCCTGTA ATAGAATCAG GGGGTCTTCT GGCTCTGGGC CCTAGAATGG 1260 GGCTGAAGCC CAGAGAGGCA GTTGCACCTC CCCTAGGCCA CACAGCAGGT ATAGGCCCCA 1320 GGGGCTGAGT GCCCATCATG CCTGCCCTCC TCTCCATCCA CCCAGAGCCT CACTAGCCAG 1380 ACCCGCACTC TCCCATCCCC TGGGCAAGTC TGCACCCCAG GTCGGTGAGG ACTCCCAGAT 1440 TCTACTCCCA CCAGCCAGGG CCAGACCTGG TGCAGGAGGC TCCACAGTTC TCCTGCTCGG 1500 GGCTCCGTCT CCCCACTTCC TGGAGCTCCA TCCAAGTGGG GAACCCTGCC CGTCCTCTGC 1560 CCCTCAAGCC AACCAGGCAT TTACGGGGGA TGGGGCAGGG AGGGAGGCCA GGACCTGCAT 1620 CCTTCCAGCC CTGGCCCTCA GCAACCCCAT CAGGCAGTCA GGGGAGGAGC CTCCCCCAGG 1680 GAATCCTCCC TCCCTCTGTG TTGGCCTGGC CAGGTTCTCC TCTCTCTGTC TGCCTTTGTC 1740 TTTTTCTCTC TGTCTCTTCA TCCCAGGAAG AGGCCACAGG ACAGGGGTGT CCCAAGCACA 1800 GAAGAAACTT GTCTGATGAA AACAGGCCTT GGCTGGGAGC AGGGCCATCT GGATTTGCAC 1860 CCTGATTCTG TCTGACTTGC TGTGTGACCT TGGGCGAGTC CCCTCCCCTC TCTGGTCTTT 1920 CCCATTATTA TCTACCCAGC ACATAGTAGG TTCTCGGAAA AGGGGAGTCA CATATGCGTG 1980 CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT TTAATCCCCA CAGATCTGCC AGCCTTTGAT 2040 ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG AATAGGAAGC TGAGGGCTCA TGGGCTGCGG 2100 GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC CTGCCCGAGG GAGGGGGCTG TGGGCCCCTC 2160 GCCATTCACT GCTAAGCCTG GATCCGGGCG CCTTTGTGCC AAGAACAAAA CCCGGGGGAT 2220 CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT CCGGAAGGGA CGGAAGCCTG GGCCTGAGGG 2280 GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG GTGCCGGGGC TGGCCCCATA CCCCAGAAGC 2340 TCCCCACTAC CTCCGGGTGT GGAGCTATGG TGGGCGAGCA AACCTGGGTT CAGATCCCAC 2400 CTTCTACTCA TCATGAGACT TGGGCAAGTG TTTTAAGCCC 2440
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