Tag | Content |
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EnhancerAtlas ID | HS128-00191 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr1:16498390-16501840 |
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 | 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: 31 | 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_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 | chr1:16496450-16499306 | 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 | CTCAGAGGGC AGAGGCTGTG GCTTCCCCAT GAGAGTGGAG GCTTCAGCAG GACAGAGGCC 60 AGGCCTCTGC TATCAGACTA GGAGCTCCCT GAGGGCAGAG GCTGTGGGAT ATTCCCGGGG 120 CAGAGGTGAC CTTCCCCCAT CAGACTGGGA CCTCAGCTCA GTCCAGCAGC TCTACGGTGA 180 ATGTCTCCGA GGGAGGGGCA TTAGCACAAC AGACACTGCC TCTCAGCCCC GAGTCCCCAG 240 ATCCATGTCA TCTATTGGAG TCTCCCCCAC TGTAAACCTG CAAGGGCAGC CACGGCCGGG 300 AGCAGCTGGT CCTGAGACTT GGGCAGAGGC CCTGGACAGT GGGGCAGAAG CGCTTGGCTG 360 GCCAGGAATT GGATCACTGC CCCCTCCCAC CCCACCCCAT TCAGCCCTGT CTCCCACGGA 420 CTCTGACCAC CCCTTGGTTC TCTTATCAAA AACCGCCAAA ACCCGCCATC GAAACTCCCA 480 GCCTCCTGAC CCCCATGCCC CACCCGGCTC CACCCGTCTT CCCAACCTGG CATCCAGTGC 540 CCCAAACCTG CCTATTCCGT TCCTGGGAAG ACCCAGAAGG GAGCAGAGCT GGCACCAGGA 600 GGCCAACAAC CCAGGCCCCC TCCGTCCCTA GCCCCTCCTG GCCCTGGGCC CTCCACCCTA 660 CTGTTTCTCC TGGGGTGTGC CTTTCTTTGC CTTATGCCTC GGCATCTCTA AGTGGCAGGG 720 GATGGAGTGG AGTGAGGGCG GCAGGCCAAG GGCATGGCCC ATAATGAAAA AGGAATCTGG 780 TTGGGCATGG TGGCTCACCC TTGTAATCTC AGCACTTTGG GAGGCCAAGG CAGGCAGATC 840 ATGAGGTCAG GAGATCGAGA GCAGCCTAGC CAACATGGTG AAACCCCGTC TCTACTAAAA 900 ACACAAAAAT TAGCTGGACG TGGTGGTGGG CGCCTGTAAT CCCAGCTACT CGGGAGGCTG 960 AGGCAGGAGA ATTGCTGGAA CCCGGGAGGT GGAGGTTGCA GTGAGCCAGG ATCACGCCAT 1020 TGCACTCCAG CTGGGGCCAA CAACAGCAAG ACTCCATCTC AAAAAAAAAA AAAAAAAAAA 1080 AGAAAAAGGA ATCTGAGCAT GGAGGCACCC TCCACCTTCG GATTGCTAGG AGATCAATGT 1140 CTGGCCCCGA GTGGGTGAGG CCAGCCGAGG TCACTTGAAG GGTATCAGCC CTGAGGAGGA 1200 GTTCACGGGG CCTCTTCCTC TCGGCCAACC CCAGCAGAGC TTGGAAACTG AGGCCCAGAG 1260 CAGGAGTCCA GGCTCATAGA GCCGGCCTGG CAGAGGAGGG GTGGGGGAGT TGCGTCCCCA 1320 CCATTCCCAC TGGGGCATAC AGCGCCTTTC TGAGCGTCAC AGGCCTGTCT GTGTCCTTCT 1380 TTTGCGGAAG AACTAACCAC ACCTCAGGTT CCCCTTATGA AAGACAGAGG CTGAGGAGAG 1440 TGAGTCAGTT TTATTATATG AGATAAGGCG GCTGGACAAA GCAGCGACAC AGGGACTGGC 1500 ACACAGACAG TGCTCAGCGA AGCAGTCGCC TTCCTTCAGG TCTGAAATCC TCACTCAGCT 1560 CCCCAGCTTC TCTGGGGGAT CTCCCTTCCC CTCTCTGGAC CCCTGGGCCT GACTTCCCCC 1620 ACTACTCCCA GCCTTTGTCC CACTCCTGCC CCAGGCACCC CTCCCTCCTT CATGGGAAAT 1680 GGAGCTTCCT CCTCTGGTCC TGCCACCACC TTCCTGGTGA GGGTCGGGCT CTGCTGGGAG 1740 TGCCAGAGCT GCCCAGCCTG CTGACTCAGC GCCTGGGGAT AGGGCTTGCT TTAGGAACAG 1800 CCCAGGCCTC GGGCAAACAG AGCCACGGCA ACCACACCCC TGCCACAGGA ATGCAGCAAC 1860 ATTCCTGGGG GGTGCCGTGG CACCGTGCCT GTGACTGGGG GGCAGGTGGG GGGCAGGTAG 1920 ACACCTGCCT CTGTTACCTT GCCACAGGTA GAAGGGAGCC AGGAGTCAGG GCCCAGTGTC 1980 CTGGGGCAGG GGGATGGAGT GAGGTCATGA GGCTTTGAAA TCTGTACCAG CCATGTGACT 2040 TGAACAAGGC CTCTCTGAGC CTCAGTTTCC TCACCTGTAA GGTGAAGGGA GAATAGCGGT 2100 AGCCTTCTGG TGGGCTTATG GGGAGGACTG AACGAGAGTG CGCCCGTCTG GGGCTCAGCA 2160 TCAGCCTGCC TCACCGTGAG GATTCCGTGA AGCAGACCCT CACCCCTGTA ATAGAATCAG 2220 GGGGTCTTCT GGCTCTGGGC CCTAGAATGG GGCTGAAGCC CAGAGAGGCA GTTGCACCTC 2280 CCCTAGGCCA CACAGCAGGT ATAGGCCCCA GGGGCTGAGT GCCCATCATG CCTGCCCTCC 2340 TCTCCATCCA CCCAGAGCCT CACTAGCCAG ACCCGCACTC TCCCATCCCC TGGGCAAGTC 2400 TGCACCCCAG GTCGGTGAGG ACTCCCAGAT TCTACTCCCA CCAGCCAGGG CCAGACCTGG 2460 TGCAGGAGGC TCCACAGTTC TCCTGCTCGG GGCTCCGTCT CCCCACTTCC TGGAGCTCCA 2520 TCCAAGTGGG GAACCCTGCC CGTCCTCTGC CCCTCAAGCC AACCAGGCAT TTACGGGGGA 2580 TGGGGCAGGG AGGGAGGCCA GGACCTGCAT CCTTCCAGCC CTGGCCCTCA GCAACCCCAT 2640 CAGGCAGTCA GGGGAGGAGC CTCCCCCAGG GAATCCTCCC TCCCTCTGTG TTGGCCTGGC 2700 CAGGTTCTCC TCTCTCTGTC TGCCTTTGTC TTTTTCTCTC TGTCTCTTCA TCCCAGGAAG 2760 AGGCCACAGG ACAGGGGTGT CCCAAGCACA GAAGAAACTT GTCTGATGAA AACAGGCCTT 2820 GGCTGGGAGC AGGGCCATCT GGATTTGCAC CCTGATTCTG TCTGACTTGC TGTGTGACCT 2880 TGGGCGAGTC CCCTCCCCTC TCTGGTCTTT CCCATTATTA TCTACCCAGC ACATAGTAGG 2940 TTCTCGGAAA AGGGGAGTCA CATATGCGTG CCCCCAGCTC TCAGCCCCTC ACTGCCTCCT 3000 TTAATCCCCA CAGATCTGCC AGCCTTTGAT ACTCCTGTGG GTGGCCGAGC CGGGGTTCTG 3060 AATAGGAAGC TGAGGGCTCA TGGGCTGCGG GGAAGCAGGC AGGGGCTGAG CCTGCCAGGC 3120 CTGCCCGAGG GAGGGGGCTG TGGGCCCCTC GCCATTCACT GCTAAGCCTG GATCCGGGCG 3180 CCTTTGTGCC AAGAACAAAA CCCGGGGGAT CAGCTGTTCT CAGGCCTGCC TCTCTCAGCT 3240 CCGGAAGGGA CGGAAGCCTG GGCCTGAGGG GTGGGCCGCA CTCCCTCCAT GGGCCCTGGG 3300 GTGCCGGGGC TGGCCCCATA CCCCAGAAGC TCCCCACTAC CTCCGGGTGT GGAGCTATGG 3360 TGGGCGAGCA AACCTGGGTT CAGATCCCAC CTTCTACTCA TCATGAGACT TGGGCAAGTG 3420 TTTTAAGCCC TCGGAGCCTC AGTTTCATGA 3450
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