Tag | Content |
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EnhancerAtlas ID | HS128-20362 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr7:44677500-44680020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr5a2 | MA0505.1 | chr7:44679698-44679713 | GCTGACCTTGACCCT | - | 6.88 |
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| Number of super-enhancer constituents: 34 | ID | Coordinate | Tissue/cell |
SE_09293 | chr7:44668114-44680616 | CD14 | SE_12002 | chr7:44675737-44680602 | CD3 | SE_14587 | chr7:44668357-44680825 | CD4_Memory_Primary_7pool | SE_15490 | chr7:44676270-44680378 | CD4_Memory_Primary_8pool | SE_16434 | chr7:44672525-44680593 | CD4_Naive_Primary_8pool | SE_16951 | chr7:44675465-44680529 | CD4p_CD225int_CD127p_Tmem | SE_17851 | chr7:44668129-44680829 | CD4p_CD25-_CD45ROp_Memory | SE_18656 | chr7:44670100-44680815 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19294 | chr7:44675433-44680659 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_20655 | chr7:44668188-44680617 | CD56 | SE_21218 | chr7:44672481-44680578 | CD8_Memory_7pool | SE_22840 | chr7:44672479-44680608 | CD8_primiary | SE_24636 | chr7:44677413-44677804 | Colon_Crypt_2 | SE_24636 | chr7:44677846-44680063 | Colon_Crypt_2 | SE_26120 | chr7:44672338-44680827 | Duodenum_Smooth_Muscle | SE_27427 | chr7:44675393-44680685 | Esophagus | SE_27654 | chr7:44668239-44680825 | Fetal_Intestine | SE_28557 | chr7:44668586-44680821 | Fetal_Intestine_Large | SE_32407 | chr7:44672719-44680093 | Gastric | SE_34691 | chr7:44670606-44681894 | HeLa | SE_36719 | chr7:44676722-44680551 | HMEC | SE_37328 | chr7:44672508-44680850 | HSMMtube | SE_40682 | chr7:44672552-44680631 | Left_Ventricle | SE_42075 | chr7:44679237-44679954 | LNCaP | SE_42544 | chr7:44672671-44680682 | Lung | SE_43768 | chr7:44675436-44680621 | MM1S | SE_46384 | chr7:44676438-44680713 | Osteoblasts | SE_48519 | chr7:44672671-44680588 | Psoas_Muscle | SE_49693 | chr7:44677999-44679961 | Right_Ventricle | SE_50531 | chr7:44677170-44680609 | Sigmoid_Colon | SE_52560 | chr7:44672691-44680563 | Small_Intestine | SE_53907 | chr7:44672618-44680662 | Spleen | SE_62947 | chr7:44653723-44680812 | Tonsil | SE_64825 | chr7:44676532-44680626 | NHEK |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 44679392 | 44679514 | chr7 | 44677628 | 44678244 | chr7 | 44678622 | 44679047 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044628 | chr7 | 44668008 | 44681598 |
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Enhancer Sequence | GTAAGAACTT CATCAGAATC CCATAGCCCC TTGCAGGGCT CAGAAGTTGG CCTTTTGGGA 60 GTGAGTGCTT TCCCGCACCC CTCCCCTGGC CCAGGACCCC TCACTCCTTC TGGCAGCTTC 120 CTGCCCCTTG AATGTCATTT ACAACCTTGC CCACTTACCT TAACATTTTA ACCTTTTCCC 180 CCTTATCAGT GACATTGTCA TTGGTGGTCA GAGAATTAAC TGTGTGTAAC TGTATATTTG 240 AGGCAAGGCA AGGGGACAGA TATTTTCCTT ACGTTATTAG TTGTGCAACA GAAGCCAATT 300 AAGAGATTGG AGAGATGAAT AACACTAGTG ATGGGTTGCA ACTTGGGTGT GGAGCTGGGC 360 ACACCCACGT ACGTCATTGT GACTCAGAAG TCCCTGTCAC CGCCCTGAGC CAAGTACTAA 420 AGTAAGGCCC AAATACCACA CTTACTTCAT AAAGAAACCA AAGTCTGACT GCCTCCATTT 480 CTCATGAGTG AAAAACTGTT TCTATTATAG GAAACTTAGG TCTTCAGTGT GTTTGATGGT 540 AGCATGCTAT TAGATTGTGT ATTCTCAAGT CTGATTTTCC CCATTACTGT GCTTTCTCCT 600 TTTCACTTCT GCTTTGTCAC TTGGAATGTT TCTAGAAGTA GAAGTCACTG CCCCTGCCTA 660 CATCAGACTG CAATTCCGGG ACATCCAGGC AACAGCAAGG GATAATTAGG AATAAATTTG 720 GCTGGAAGAA AGGGAAAATG CAGCTTAGGC AGCCTAAACC AACAGGCTTA TTTTTCTCAC 780 TCAGTAAGAG AGCTGAGGTC GCCTGACTCA GCTCAGGTTC TCAGTGAGCC ATCAGCCACC 840 AGGTGCCACC TTTCAGTGAG TGGGCTTCTA TCCCTTCCAG GTGTCTCTTC ATGCTCCATG 900 GGAATTAGAT GGGACATGCT TTGACTCTCT CTTCCAGAAG CTTTCTCTTC TTTTTGAAGG 960 GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT CTTGATTTAT CCCCCAGGAT 1020 GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG TGTACAGTAA GGGCTGGGAG 1080 TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT AAGCGACCAT GTGAAGGGAG 1140 AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC TGCGGGAAGG AAGGAGCATG 1200 ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC AGGTCCCCTG GAACCTAAAG 1260 CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG AGGATGAGGC AGGGGTGGGT 1320 AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG GAAGATGTTA GAGAGATACA 1380 GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA TGGACTGTGG CATCTGGGCC 1440 CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG GAGGGGTGGG GCCAGTGGGT 1500 GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC TGCCACATCT GTTGGGAGGT 1560 GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC TTTTTGAATA AATAAACTTT 1620 TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT AAGTGTTTAG TGCAGTAGGT 1680 TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA TTCTATCACT CAATTCAAAA 1740 ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT GGGTGTGGGG 1800 GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA AGGTGGGGCA GGGTGCTCCC 1860 CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG GATGCATGGT GTAAGATGAA 1920 TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC TTCCCGGGGA TTCCCAGCAG 1980 CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC TCCAGCATGA GCTGAATTTC 2040 CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG AGTTGTATTC CAAGCACAAA 2100 AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC TGTCTCCAGG GCCTAGGCTG 2160 GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC TGACCTTGAC CCTGACCTTG 2220 TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA TTGTTGAGCC CAGAAGCGCC 2280 CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT GTTACTAGAG TGACCAGAGT 2340 TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT AATACCCTGC CTGGTGACTG 2400 CTGTGTGTAA ATTCTGCCTG AGCCCACATC TCTCCAGTGG GAATATGATT GACATTCCAG 2460 GTGCTCTAAG TAAGTTGGAA AAGCCCACAG AGAGCCTCAG TAAAAGTTAG CTATACCTAT 2520
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