Tag | Content |
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EnhancerAtlas ID | HS162-09491 |
Organism | Homo sapiens |
Tissue/cell | Plasma_cell_myeloma |
Coordinate | chr7:44677440-44680220 |
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: 35 | 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 | chr7:44677432-44677748 | Right_Ventricle | 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 | ATTTTTTGAC ATGGTACATC CTGCACACAT CTGACACTCT TAGGAAAATG TTTATGTGTG 60 GTAAGAACTT CATCAGAATC CCATAGCCCC TTGCAGGGCT CAGAAGTTGG CCTTTTGGGA 120 GTGAGTGCTT TCCCGCACCC CTCCCCTGGC CCAGGACCCC TCACTCCTTC TGGCAGCTTC 180 CTGCCCCTTG AATGTCATTT ACAACCTTGC CCACTTACCT TAACATTTTA ACCTTTTCCC 240 CCTTATCAGT GACATTGTCA TTGGTGGTCA GAGAATTAAC TGTGTGTAAC TGTATATTTG 300 AGGCAAGGCA AGGGGACAGA TATTTTCCTT ACGTTATTAG TTGTGCAACA GAAGCCAATT 360 AAGAGATTGG AGAGATGAAT AACACTAGTG ATGGGTTGCA ACTTGGGTGT GGAGCTGGGC 420 ACACCCACGT ACGTCATTGT GACTCAGAAG TCCCTGTCAC CGCCCTGAGC CAAGTACTAA 480 AGTAAGGCCC AAATACCACA CTTACTTCAT AAAGAAACCA AAGTCTGACT GCCTCCATTT 540 CTCATGAGTG AAAAACTGTT TCTATTATAG GAAACTTAGG TCTTCAGTGT GTTTGATGGT 600 AGCATGCTAT TAGATTGTGT ATTCTCAAGT CTGATTTTCC CCATTACTGT GCTTTCTCCT 660 TTTCACTTCT GCTTTGTCAC TTGGAATGTT TCTAGAAGTA GAAGTCACTG CCCCTGCCTA 720 CATCAGACTG CAATTCCGGG ACATCCAGGC AACAGCAAGG GATAATTAGG AATAAATTTG 780 GCTGGAAGAA AGGGAAAATG CAGCTTAGGC AGCCTAAACC AACAGGCTTA TTTTTCTCAC 840 TCAGTAAGAG AGCTGAGGTC GCCTGACTCA GCTCAGGTTC TCAGTGAGCC ATCAGCCACC 900 AGGTGCCACC TTTCAGTGAG TGGGCTTCTA TCCCTTCCAG GTGTCTCTTC ATGCTCCATG 960 GGAATTAGAT GGGACATGCT TTGACTCTCT CTTCCAGAAG CTTTCTCTTC TTTTTGAAGG 1020 GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT CTTGATTTAT CCCCCAGGAT 1080 GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG TGTACAGTAA GGGCTGGGAG 1140 TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT AAGCGACCAT GTGAAGGGAG 1200 AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC TGCGGGAAGG AAGGAGCATG 1260 ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC AGGTCCCCTG GAACCTAAAG 1320 CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG AGGATGAGGC AGGGGTGGGT 1380 AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG GAAGATGTTA GAGAGATACA 1440 GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA TGGACTGTGG CATCTGGGCC 1500 CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG GAGGGGTGGG GCCAGTGGGT 1560 GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC TGCCACATCT GTTGGGAGGT 1620 GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC TTTTTGAATA AATAAACTTT 1680 TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT AAGTGTTTAG TGCAGTAGGT 1740 TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA TTCTATCACT CAATTCAAAA 1800 ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT GGGTGTGGGG 1860 GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA AGGTGGGGCA GGGTGCTCCC 1920 CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG GATGCATGGT GTAAGATGAA 1980 TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC TTCCCGGGGA TTCCCAGCAG 2040 CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC TCCAGCATGA GCTGAATTTC 2100 CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG AGTTGTATTC CAAGCACAAA 2160 AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC TGTCTCCAGG GCCTAGGCTG 2220 GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC TGACCTTGAC CCTGACCTTG 2280 TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA TTGTTGAGCC CAGAAGCGCC 2340 CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT GTTACTAGAG TGACCAGAGT 2400 TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT AATACCCTGC CTGGTGACTG 2460 CTGTGTGTAA ATTCTGCCTG AGCCCACATC TCTCCAGTGG GAATATGATT GACATTCCAG 2520 GTGCTCTAAG TAAGTTGGAA AAGCCCACAG AGAGCCTCAG TAAAAGTTAG CTATACCTAT 2580 CCCTGCTGCT ATTGGTGGGT TTTTTTTGTT TTGTTTTGTT TTACTATTTT AATTGTTATT 2640 CAAAGCTAAT TTTATTGAAA AGAAGTAAAC TTGTGATTTT GCTATGACTT TTGGCTCTGG 2700 ATCCAAAAGT GAATATTGTC CCCTAGGATA AAGGAGGCTG TCTGTACAGC TGGAGAGACT 2760 CTTGATCTAA GGTCTTGCTC 2780
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