Tag | Content |
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EnhancerAtlas ID | HS177-20802 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH_RA |
Coordinate | chr7:44678730-44679980 |
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: 33 | 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 | chr7:44677846-44680063 | 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: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044628 | chr7 | 44668008 | 44681598 |
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Enhancer Sequence | AGGGCTCTGC AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC 60 AGGTGTTCAG AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC 120 TTGGGGAGTG GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA 180 GAGTGGGGGA TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA 240 CTCATACAGG GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT 300 GGCTTCCTGC TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT 360 TTTCAAAGCC TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT 420 CACTTGTTTT AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG 480 ATACAAAACA TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC 540 AAAGAGGGCT TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT 600 CTTTGTCTGA AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG 660 AGTGAAGTGG GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC 720 AGCATTTTCC TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT 780 TCTGACTGCC TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA 840 AATCACCTGG AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC 900 ATGATCGCCC TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG 960 ACCAGAGAGC TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC 1020 TTTCATTTTA TTGTTGAGCC CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT 1080 AAGAGGCACT GTTACTAGAG TGACCAGAGT TCTTTAAGCG TCGCTCTGCT ATTACTCAGT 1140 TAACCTTATT AATACCCTGC CTGGTGACTG CTGTGTGTAA ATTCTGCCTG AGCCCACATC 1200 TCTCCAGTGG GAATATGATT GACATTCCAG GTGCTCTAAG TAAGTTGGAA 1250
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