Tag | Content |
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EnhancerAtlas ID | HS034-27736 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr7:44678450-44679920 |
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 | TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT CTTGATTTAT 60 CCCCCAGGAT GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG TGTACAGTAA 120 GGGCTGGGAG TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT AAGCGACCAT 180 GTGAAGGGAG AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC TGCGGGAAGG 240 AAGGAGCATG ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC AGGTCCCCTG 300 GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG AGGATGAGGC 360 AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG GAAGATGTTA 420 GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA TGGACTGTGG 480 CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG GAGGGGTGGG 540 GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC TGCCACATCT 600 GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC TTTTTGAATA 660 AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT AAGTGTTTAG 720 TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA TTCTATCACT 780 CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT 840 GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA AGGTGGGGCA 900 GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG GATGCATGGT 960 GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC TTCCCGGGGA 1020 TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC TCCAGCATGA 1080 GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG AGTTGTATTC 1140 CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC TGTCTCCAGG 1200 GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC TGACCTTGAC 1260 CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA TTGTTGAGCC 1320 CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT GTTACTAGAG 1380 TGACCAGAGT TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT AATACCCTGC 1440 CTGGTGACTG CTGTGTGTAA ATTCTGCCTG 1470
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