Tag | Content |
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EnhancerAtlas ID | HS089-11495 |
Organism | Homo sapiens |
Tissue/cell | Hela |
Coordinate | chr7:44678380-44679750 |
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: 2 | Chromosome | Start | End |
chr7 | 44679392 | 44679514 | chr7 | 44678622 | 44679047 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044628 | chr7 | 44668008 | 44681598 |
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Enhancer Sequence | GTGTCTCTTC ATGCTCCATG GGAATTAGAT GGGACATGCT TTGACTCTCT CTTCCAGAAG 60 CTTTCTCTTC TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT 120 CTTGATTTAT CCCCCAGGAT GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG 180 TGTACAGTAA GGGCTGGGAG TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT 240 AAGCGACCAT GTGAAGGGAG AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC 300 TGCGGGAAGG AAGGAGCATG ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC 360 AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG 420 AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG 480 GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA 540 TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG 600 GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC 660 TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC 720 TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT 780 AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA 840 TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT 900 TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA 960 AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG 1020 GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC 1080 TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC 1140 TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG 1200 AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC 1260 TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC 1320 TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC 1370
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