Tag | Content |
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EnhancerAtlas ID | HS130-02490 |
Organism | Homo sapiens |
Tissue/cell | MDA-MB-231 |
Coordinate | chr1:201987100-201989280 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Klf1 | MA0493.1 | chr1:201988332-201988343 | AGCCACACCCA | + | 6.14 | NR2C2 | MA0504.1 | chr1:201987451-201987466 | TGCCCTCTCACCCCT | - | 6.45 | NR2C2 | MA0504.1 | chr1:201987162-201987177 | TGACCTTTGCCCTGC | - | 6.4 | Nr2f6 | MA0677.1 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.45 | RARA(var.2) | MA0730.1 | chr1:201987749-201987766 | AGGTCAGAGGGAGGTCA | + | 6.41 | REST | MA0138.2 | chr1:201988024-201988045 | CTCAGCACCTTGCACAGCGCC | + | 7.87 | Rxra | MA0512.2 | chr1:201987162-201987176 | TGACCTTTGCCCTG | - | 6.09 | Zfx | MA0146.2 | chr1:201988564-201988578 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_23058 | chr1:201986872-201988608 | Colon_Crypt_1 | SE_23058 | chr1:201988689-201989148 | Colon_Crypt_1 | SE_23723 | chr1:201986912-201988613 | Colon_Crypt_2 | SE_23723 | chr1:201988825-201989067 | Colon_Crypt_2 | SE_24689 | chr1:201986888-201988638 | Colon_Crypt_3 | SE_24689 | chr1:201988803-201989120 | Colon_Crypt_3 | SE_25977 | chr1:201976074-201988947 | Duodenum_Smooth_Muscle | SE_26730 | chr1:201985712-201988797 | Esophagus | SE_27624 | chr1:201975812-201989193 | Fetal_Intestine | SE_28545 | chr1:201974530-201989440 | Fetal_Intestine_Large | SE_31432 | chr1:201983938-201989177 | Gastric | SE_33417 | chr1:201986876-201989229 | H2171 | SE_33792 | chr1:201978127-201990221 | HCC1954 | SE_34304 | chr1:201974676-201989923 | HCT-116 | SE_34741 | chr1:201985668-201989981 | HeLa | SE_41626 | chr1:201986861-201988608 | LNCaP | SE_41626 | chr1:201988805-201989112 | LNCaP | SE_43434 | chr1:201986862-201988630 | MCF-7 | SE_43434 | chr1:201988714-201989565 | MCF-7 | SE_47796 | chr1:201986886-201988593 | Pancreas | SE_50066 | chr1:201978058-201988672 | Sigmoid_Colon | SE_52354 | chr1:201976011-201988714 | Small_Intestine | SE_52354 | chr1:201988740-201989300 | Small_Intestine | SE_56834 | chr1:201986879-201988600 | VACO_400 | SE_56834 | chr1:201988818-201989093 | VACO_400 | SE_57376 | chr1:201986910-201988595 | VACO_503 | SE_57945 | chr1:201986912-201988581 | VACO_9m | SE_57945 | chr1:201988821-201989091 | VACO_9m | SE_65333 | chr1:201986253-201989108 | Pancreatic_islets | SE_67013 | chr1:201986876-201989229 | H2171 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 201987200 | 201988600 | chr1 | 201987611 | 201988279 |
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Enhancer Sequence | ATGGCGCTCA GCCCCTTCAC CCTCTTCTGG AGGGCTGGGG GCAGGTGCTG CCCGCTGCGT 60 GCTGACCTTT GCCCTGCCAT TTGCAGTTTA TGAGGCGCTT TCCTCATCCC ATTATCTCAT 120 TTGATCCGCC CCACAGCTCG CTGAGGAGAC CAGGTGTCCC CATTTTACTG ACAAGGCTAG 180 TGGTGGGCTG AAGTCACTGA CTGGGTGAGA GCGGGGCCAG CTCACAGCAT GCCTGCCTCC 240 ACGCTGCAGC TCAGTGAGAC CACCTGGGCA GGTGGCCTCT GCAGGGCAGC GCCTGGGACA 300 GCCTGGAAGA CGGCAGCTCT GGGAGGGACG CCTTTCTCCC CAACAGTTCT CTGCCCTCTC 360 ACCCCTCAGG ATGCTGCAGA GTCCTGGCAC GGGCCCCTGG GCTGGCCTCC GTGCTGCCCT 420 CTCTGTCGGG CACCAGTCAC CCTTACCCCG ACTCTCACCA GCCCAGGGGC CTCCTAGCAG 480 GAGACGGCCC GGTCTCTCGC CCACCAGAGT CTGCATCCCC TCAGGTGTGT CCTGGGCTGG 540 GGAGTGGGGG TGGGGAGGAA GCCACAGGGC CGGGCTGTTT ATATCCCGCC CTGCCGGAGC 600 TGCTGGTCAC CTCTTATCTG CTTCTGTGGG ATTGGGTGTG TCGCTGAGCA GGTCAGAGGG 660 AGGTCACCCC TCCCGTCGTG TTTGGGTGTG CCTGAGGAGG GGCTGGGGTT GGCCCCCTGG 720 GACAGTTCCT GGCTTATCCC ACAGCCCCAC CTGTCCCACC AATTCTGGGG AAGTCTGGCT 780 TCTCCTGGGG GAAGTGGGTG AAGGGGTTGC ATTTCTGAGG AGTCTGGTTT CAATCTGCTC 840 TCTCTCTCTG CTGTTGTCTG TTTACACATC TCTCTCTCTC GCCGGGCTGT GAGCACCTCT 900 GGGCAAGTGC TGGGGCTTAC TCACCTCAGC ACCTTGCACA GCGCCTGGCA CAGAGGAGGT 960 GCTCGATAAA TATTTGCTAA ATGGCCCCGT GACTCTCCCT GCCCTGGCCA CTACCTCCCC 1020 CACACACCAC ACACATTCAT ACACACTCAT GGGAACCAAA GTCACACACA CTCACACTCA 1080 CAAAGATAAA TATTCACAAG CCCTCACTCA CATGCCCCTG CACGCACTGC AGACGCTGCC 1140 TGCTCTCACA CACTCGCATG GACCGTATTC ACAACCTCAC ACACTTGCAC ACACCAGCGC 1200 ACGCAACACA CTCCCACCTC ACAGTCTCAC ATAGCCACAC CCAGGCCTGC CTGCACGACT 1260 CACCTCCTCC CTCGGGGTCC TTCTATGAAG CATTTCCTGA CCTCCTCTTT GGCCCTTTTC 1320 CCCCACCAGA TGGGTTCAGC CCTTGCCTCC AGTCAGGACA GGCCTGGTAA TTTGCAGAGC 1380 CCAGTGCAAA GTGAAAGCCT GGGCCCTTGT TAAAGAATTA TTAGGCTGGG CGCAGTGGCT 1440 CATGCCAGTA ATCCCACACT TTGGGAGGCC GAGGCGGGTG GATCGCCTGA GGTCAGGAGT 1500 TTGAGACCAG CCTGACCAAC ATGGCGAAAC CCCATCTCTA CTAAAAATAC AAAATTAGCT 1560 GGGCGTGGTG GTGTGCGCCT GTAATCCTAG CTACTCTGGA GGTTGAGGCA GAAGAATCGC 1620 TTGAACCTGG GAGGCGGAGG TTGCCGTGAA CCAAGATCAT GACACTGCAC TCCCGCCTGG 1680 GCAACAAGAG AGAAACTCCA TCTCAAAAAA AAAAAAAAAA AAGAACGATT AAAAATTTCA 1740 AAATGGCAAC AGCAGAGAAG AGCATGAACC ATGCGCGAGG TGCAGTCCTC CAAGCGCAGG 1800 GCCCTGTGGG ACCACCGCAC AGGTTGCACT CAGGAAGCCA CCCCTGCCTC CATTTGCCAC 1860 TGGCCTATAA GAGCTCCACT GAACTACCCA CCATGCCTTC TACTACAGAT ATGTTTGCCA 1920 CAGTCACAAA AAAATCAACA AGTTGTCAAG TTTTTTGCTT TTTGTTTTTG AGACGGAGTC 1980 ATGCTCTGTC CCCCAGGCTG GAGTGCAGTG GTGCCATCTC GGCTCACTGA AACCTCTGCC 2040 TCCCGGGTTC ACACCATTCT CCTGCCTCAG CCTCCTGAGT AGCTGGGACT ACAGGCGCCC 2100 ATGACCACGC CCGACTAATT TTTTGCATTT TTAGTAGAGA TGGGGTTTCA CTGTGTTAGC 2160 CAGGATGGTC TCGATCCCCT 2180
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