Tag | Content |
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EnhancerAtlas ID | HS044-12064 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr7:44678750-44680100 |
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 | GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG AGGATGAGGC 60 AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG GAAGATGTTA 120 GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA TGGACTGTGG 180 CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG GAGGGGTGGG 240 GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC TGCCACATCT 300 GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC TTTTTGAATA 360 AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT AAGTGTTTAG 420 TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA TTCTATCACT 480 CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT 540 GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA AGGTGGGGCA 600 GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG GATGCATGGT 660 GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC TTCCCGGGGA 720 TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC TCCAGCATGA 780 GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG AGTTGTATTC 840 CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC TGTCTCCAGG 900 GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC TGACCTTGAC 960 CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA TTGTTGAGCC 1020 CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT GTTACTAGAG 1080 TGACCAGAGT TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT AATACCCTGC 1140 CTGGTGACTG CTGTGTGTAA ATTCTGCCTG AGCCCACATC TCTCCAGTGG GAATATGATT 1200 GACATTCCAG GTGCTCTAAG TAAGTTGGAA AAGCCCACAG AGAGCCTCAG TAAAAGTTAG 1260 CTATACCTAT CCCTGCTGCT ATTGGTGGGT TTTTTTTGTT TTGTTTTGTT TTACTATTTT 1320 AATTGTTATT CAAAGCTAAT TTTATTGAAA 1350
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