Tag | Content |
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EnhancerAtlas ID | HS159-05632 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr7:44677940-44680600 |
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: 34 | 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_32407 | chr7:44680106-44680586 | 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: 3 | Chromosome | Start | End |
chr7 | 44679392 | 44679514 | chr7 | 44680101 | 44680272 | chr7 | 44678622 | 44679047 |
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| Number: 1 | ID | Chromosome | Start | End |
GH07I044628 | chr7 | 44668008 | 44681598 |
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Enhancer Sequence | CTTACTTCAT AAAGAAACCA AAGTCTGACT GCCTCCATTT CTCATGAGTG AAAAACTGTT 60 TCTATTATAG GAAACTTAGG TCTTCAGTGT GTTTGATGGT AGCATGCTAT TAGATTGTGT 120 ATTCTCAAGT CTGATTTTCC CCATTACTGT GCTTTCTCCT TTTCACTTCT GCTTTGTCAC 180 TTGGAATGTT TCTAGAAGTA GAAGTCACTG CCCCTGCCTA CATCAGACTG CAATTCCGGG 240 ACATCCAGGC AACAGCAAGG GATAATTAGG AATAAATTTG GCTGGAAGAA AGGGAAAATG 300 CAGCTTAGGC AGCCTAAACC AACAGGCTTA TTTTTCTCAC TCAGTAAGAG AGCTGAGGTC 360 GCCTGACTCA GCTCAGGTTC TCAGTGAGCC ATCAGCCACC AGGTGCCACC TTTCAGTGAG 420 TGGGCTTCTA TCCCTTCCAG GTGTCTCTTC ATGCTCCATG GGAATTAGAT GGGACATGCT 480 TTGACTCTCT CTTCCAGAAG CTTTCTCTTC TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT 540 GGTCAATGAC TCAGCCTAGT CTTGATTTAT CCCCCAGGAT GGGGACAGAC AGCAGGGGAG 600 AGATCTCAGG TTGAGATGAG TGTACAGTAA GGGCTGGGAG TATCAGAAGG GGAAACGCTC 660 TCCCAGATAG TGACAAAGCT AAGCGACCAT GTGAAGGGAG AGGACAAACA TCCCATGGAA 720 AGAAGGGTAG CTGCCAGGCC TGCGGGAAGG AAGGAGCATG ATGCTGGGGC ATGGGAGCAA 780 GTGGACAGGG AGGGCTCTGC AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG 840 ATCCAGATTC AGGTGTTCAG AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG 900 AGGTATCTCC TTGGGGAGTG GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA 960 GGTGGAAAGA GAGTGGGGGA TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC 1020 CCATTGGTGA CTCATACAGG GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT 1080 GGGCAGGTCT GGCTTCCTGC TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA 1140 TGACCTTCAT TTTCAAAGCC TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA 1200 TATTAAAATT CACTTGTTTT AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC 1260 ACTACACTCG ATACAAAACA TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG 1320 GTCTTGGCGC AAAGAGGGCT TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC 1380 AGAATGGGCT CTTTGTCTGA AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG 1440 CCAACTGGAG AGTGAAGTGG GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG 1500 TTGCATTCCC AGCATTTTCC TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA 1560 CCAGTTTTTT TCTGACTGCC TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA 1620 GCCAATTGAA AATCACCTGG AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG 1680 CCCGATGATC ATGATCGCCC TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT 1740 GTGGCTCAGG ACCAGAGAGC TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC 1800 TGGAAATTCC TTTCATTTTA TTGTTGAGCC CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT 1860 AAGCTAGGGT AAGAGGCACT GTTACTAGAG TGACCAGAGT TCTTTAAGCG TCGCTCTGCT 1920 ATTACTCAGT TAACCTTATT AATACCCTGC CTGGTGACTG CTGTGTGTAA ATTCTGCCTG 1980 AGCCCACATC TCTCCAGTGG GAATATGATT GACATTCCAG GTGCTCTAAG TAAGTTGGAA 2040 AAGCCCACAG AGAGCCTCAG TAAAAGTTAG CTATACCTAT CCCTGCTGCT ATTGGTGGGT 2100 TTTTTTTGTT TTGTTTTGTT TTACTATTTT AATTGTTATT CAAAGCTAAT TTTATTGAAA 2160 AGAAGTAAAC TTGTGATTTT GCTATGACTT TTGGCTCTGG ATCCAAAAGT GAATATTGTC 2220 CCCTAGGATA AAGGAGGCTG TCTGTACAGC TGGAGAGACT CTTGATCTAA GGTCTTGCTC 2280 TTGGGTGACT TTGCCCTGTG TTTCTGGACA CTTAATGGGT TTTACGAAAT AGAAGAAAAT 2340 GTTTTAGGGG TTTAATAAAG TTTGGGTTGT GCTGTTCTCC AGTACTTACT GGGTTTGAGG 2400 GTCATGCCCT ATCCATGAAC CTGTTGTGGC CCCAGGGAAC TAAGTAAGTG TCTACAGCTA 2460 GACTTGGGGT GCGGGTCACA TGGTGTGAGG GTAGACATTC TAGCACTGGA GCAAGTTTGG 2520 GGTAAAGAAA AATTTTGATT AGGTTTTTTG TGGGTTTTTT TTTTTTTCTT TGAGACAGAG 2580 TCTCGCTCTG TCGCCAAACT GGAGTGCAAT GGCATGATCT CAGCTCACTG CAACCTCCGA 2640 CTCCCTGGTT CAAGTGATTG 2660
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