Tag | Content |
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EnhancerAtlas ID | HS158-51732 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr7:44678080-44680020 |
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 | CCATTACTGT GCTTTCTCCT TTTCACTTCT GCTTTGTCAC TTGGAATGTT TCTAGAAGTA 60 GAAGTCACTG CCCCTGCCTA CATCAGACTG CAATTCCGGG ACATCCAGGC AACAGCAAGG 120 GATAATTAGG AATAAATTTG GCTGGAAGAA AGGGAAAATG CAGCTTAGGC AGCCTAAACC 180 AACAGGCTTA TTTTTCTCAC TCAGTAAGAG AGCTGAGGTC GCCTGACTCA GCTCAGGTTC 240 TCAGTGAGCC ATCAGCCACC AGGTGCCACC TTTCAGTGAG TGGGCTTCTA TCCCTTCCAG 300 GTGTCTCTTC ATGCTCCATG GGAATTAGAT GGGACATGCT TTGACTCTCT CTTCCAGAAG 360 CTTTCTCTTC TTTTTGAAGG GGCTTCTGTT TGCGCTGGGT GGTCAATGAC TCAGCCTAGT 420 CTTGATTTAT CCCCCAGGAT GGGGACAGAC AGCAGGGGAG AGATCTCAGG TTGAGATGAG 480 TGTACAGTAA GGGCTGGGAG TATCAGAAGG GGAAACGCTC TCCCAGATAG TGACAAAGCT 540 AAGCGACCAT GTGAAGGGAG AGGACAAACA TCCCATGGAA AGAAGGGTAG CTGCCAGGCC 600 TGCGGGAAGG AAGGAGCATG ATGCTGGGGC ATGGGAGCAA GTGGACAGGG AGGGCTCTGC 660 AGGTCCCCTG GAACCTAAAG CCAGGGGTTA TGGAAGGCAG ATCCAGATTC AGGTGTTCAG 720 AGGATGAGGC AGGGGTGGGT AGTTTAAGGA GCTGGAGAAG AGGTATCTCC TTGGGGAGTG 780 GAAGATGTTA GAGAGATACA GGGTTGCAGG ACAACAGGGA GGTGGAAAGA GAGTGGGGGA 840 TGGACTGTGG CATCTGGGCC CCACCAGGAA GGAAGTGGCC CCATTGGTGA CTCATACAGG 900 GAGGGGTGGG GCCAGTGGGT GCCTGGGAGC TCTGGTACTT GGGCAGGTCT GGCTTCCTGC 960 TGCCACATCT GTTGGGAGGT GAAGCCTGCA GGCCAAATAA TGACCTTCAT TTTCAAAGCC 1020 TTTTTGAATA AATAAACTTT TTTGAGGTTT AACTTACATA TATTAAAATT CACTTGTTTT 1080 AAGTGTTTAG TGCAGTAGGT TTTGCCAAAT GTGTGCAGTC ACTACACTCG ATACAAAACA 1140 TTCTATCACT CAATTCAAAA ACCTTTTAGT ATACCTCCAG GTCTTGGCGC AAAGAGGGCT 1200 TGCTGTTGTT GGGTGTGGGG GCTCACCCAG TCCTGGAGAC AGAATGGGCT CTTTGTCTGA 1260 AGGTGGGGCA GGGTGCTCCC CCAGTGGTGT GGGAACTGAG CCAACTGGAG AGTGAAGTGG 1320 GATGCATGGT GTAAGATGAA TAAGGGAAAG GCTGCAGAAG TTGCATTCCC AGCATTTTCC 1380 TTCCCGGGGA TTCCCAGCAG CTCAGCAGTA CCGGTATGAA CCAGTTTTTT TCTGACTGCC 1440 TCCAGCATGA GCTGAATTTC CGTCTGTGCA GTTATCCTCA GCCAATTGAA AATCACCTGG 1500 AGTTGTATTC CAAGCACAAA AGAAGGTCAG AGAGTGGAGG CCCGATGATC ATGATCGCCC 1560 TGTCTCCAGG GCCTAGGCTG GAAGGAGTCC TGCAGCCTTT GTGGCTCAGG ACCAGAGAGC 1620 TGACCTTGAC CCTGACCTTG TGATCCCAGG CATCAGTGGC TGGAAATTCC TTTCATTTTA 1680 TTGTTGAGCC CAGAAGCGCC CAGCTCTCTT TGGCAAGGTT AAGCTAGGGT AAGAGGCACT 1740 GTTACTAGAG TGACCAGAGT TCTTTAAGCG TCGCTCTGCT ATTACTCAGT TAACCTTATT 1800 AATACCCTGC CTGGTGACTG CTGTGTGTAA ATTCTGCCTG AGCCCACATC TCTCCAGTGG 1860 GAATATGATT GACATTCCAG GTGCTCTAAG TAAGTTGGAA AAGCCCACAG AGAGCCTCAG 1920 TAAAAGTTAG CTATACCTAT 1940
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