Tag | Content |
---|
EnhancerAtlas ID | HS105-67692 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr6:7156320-7158860 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF2 | MA0051.1 | chr6:7158510-7158528 | GTTCAGGTTTAACTTTCC | - | 6.08 | Lhx3 | MA0135.1 | chr6:7157358-7157371 | GACTAATTAATTA | - | 6.46 | POU4F2 | MA0683.1 | chr6:7157356-7157372 | ATGACTAATTAATTAG | + | 6.31 | mix-a | MA0621.1 | chr6:7157362-7157373 | AATTAATTAGT | + | 6.62 | mix-a | MA0621.1 | chr6:7157359-7157370 | ACTAATTAATT | - | 6.62 |
|
| Number of super-enhancer constituents: 32 | ID | Coordinate | Tissue/cell |
SE_00099 | chr6:7150760-7175124 | Adipose_Nuclei | SE_01064 | chr6:7156909-7157399 | Adrenal_Gland | SE_09175 | chr6:7150259-7157560 | CD14 | SE_09175 | chr6:7157614-7160672 | CD14 | SE_11591 | chr6:7151171-7157857 | CD20 | SE_13456 | chr6:7152346-7157404 | CD34_Primary_RO01536 | SE_19023 | chr6:7153632-7157082 | CD4p_CD25-_Il17-_PMAstim_Th | SE_23267 | chr6:7158358-7158959 | Colon_Crypt_1 | SE_24175 | chr6:7156917-7157366 | Colon_Crypt_2 | SE_26179 | chr6:7155827-7157592 | Duodenum_Smooth_Muscle | SE_26569 | chr6:7156004-7159037 | Esophagus | SE_30159 | chr6:7153789-7157484 | Fetal_Muscle | SE_31247 | chr6:7155792-7156986 | Fetal_Thymus | SE_31471 | chr6:7156479-7157355 | Gastric | SE_31471 | chr6:7157812-7159002 | Gastric | SE_32706 | chr6:7152529-7158442 | GM12878 | SE_35642 | chr6:7157804-7163763 | HepG2 | SE_37264 | chr6:7153761-7159594 | HSMMtube | SE_41219 | chr6:7156041-7157496 | Left_Ventricle | SE_42377 | chr6:7156013-7157585 | Lung | SE_42377 | chr6:7157749-7158821 | Lung | SE_43730 | chr6:7154650-7157540 | MM1S | SE_45215 | chr6:7156500-7157614 | NHLF | SE_46025 | chr6:7155667-7160190 | Osteoblasts | SE_50177 | chr6:7156036-7157572 | Sigmoid_Colon | SE_51588 | chr6:7153835-7157377 | Skeletal_Muscle | SE_51921 | chr6:7153969-7159058 | Skeletal_Muscle_Myoblast | SE_52972 | chr6:7155944-7157485 | Small_Intestine | SE_53741 | chr6:7156781-7157462 | Spleen | SE_54903 | chr6:7155996-7157477 | Stomach_Smooth_Muscle | SE_59725 | chr6:7099938-7157593 | Ly4 | SE_63714 | chr6:7153896-7159166 | HSMM |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH06I007150 | chr6 | 7150768 | 7159561 |
|
Enhancer Sequence | AAGCCAGGGC TTAACCACGG GGTTTTTTCT CATTCACACT TAAGAGTCTA GACTTTTCGT 60 TTGAGAAGCA GTTGCTTGTC TTGGAGTTTA GTAATTGAAG GGAACAGAGG TGGGAGAGGG 120 AGGAAATTAT TTGCATAAGT TGTTTTAAAG CTCCGTCCAC TTCCTTTCCC TTCATCACTT 180 TAAATGGTTT AATTTGCTTA GGTACTTCAG CAGAGGTGTA GATAATTGAG GTAAATCTCG 240 AGTCAAATCT AAACAAAAGA AAGAACTGAC CTAAAAAAGA GCAACTGAAC TCACACTAAT 300 TGAATCACAG ATTTGCTCAG ACCAATCTAA CCTGTGAGGA AGGCCAGGGA ACACTGTGCC 360 CTTGATGTGC TTTTTGCCTC TTAAGAGGGA ACACCAGCCA GTCCCTTGTG GCTCTCCCAG 420 CCACCTTCCG CACTGAGCCA CATCTGGGTT AGAGCTGCAA AATTCACCCT GAAAAAAATG 480 TGAAAGCCAT TTTGGGTTGG ACATTTGTAA AACAAATTTT TTCTCCTTTT GGAGACCTGG 540 TGCCCTTGGT ATTTGTATAT AGAATCCACT TGTTTATTCT TGAGGAGAGC AGCTATGTGT 600 GTGAATTGGG CATCCGTTGG AAGAAACATA ACAGGCTTGC CTGTAACAGC TGGAATATAG 660 TTGCAGCCCT TTGAAATAAG ACAATCTTAG TTTTCCTTCC TTCTCCTTAG CCAGCCATCC 720 AGCGTAGGAA ACAGGATGCT GTGTACGTAC CCTGAGTAGG AGGAGAGGGT TCCAGAGTGC 780 CACTTGGCTG CTCCTGTGTA CCCATTCTTG TTCAAGAGCA CCTTGAGATC ACATGGTCTT 840 AAATGCCAAA GCTGACCAAG AGCTGCCCCT CTGTTCAGCT TCGTCGTCCC TGGCTGTTGG 900 GGAGGACTTT GTCTGTCTGA CTGCCGCTGG GCTGCCTTGC CCCAGCTCCC TGGGGTCCTT 960 TGCTCCGTAA TCCATCAGCT CTTCTTTTCT CTTCTTCTTA CTCATAGTAT AAGACCCGAC 1020 TGCCCATTTT TTGGAGATGA CTAATTAATT AGTAAAATAT TTGGCTGGGC GCGGTGGCTC 1080 ACGTCTGAAA TCCCAGCACT TTGGGATGCA GAGGCAGGCA GATGGCTTGA GTTCAGGAAG 1140 TTGGAGACCA GCCTAGGCAA CATGGTGAAA CCCTGTCTCT ACCAAAAATA CAAAAACTTA 1200 GCCAGGTGTG GTGGGGCGTG CCTGTAGTCC CAGCCACTTA GGAGGCTGAG GCACAAGAAT 1260 TGCTTGAACC CGGGAGGTGG AGGTTGTAGT GAGCCAAGAT CGTGCAGCTG CACTCCAGCC 1320 TGGGCAACAG AGTAAGACTC CATCTCAAAA AAAAAAAAAA TTGAGTGCCT ACTGTGTGCA 1380 CATGTACCCT GTGTGACCAT GGGCCAGGCA CAGTGGTTCA TGCCTGTAAT CCCAGCACTT 1440 TGAGAGGCTG AAGCAGGTGG ATTGCTCGAG CCCAGGAGTT CGAGACCAGC CTGGGCAACA 1500 TAGTGAGACT CCGTCTCTCC AAAAAAAAAA TAAAGTTAGC ATGGTGTGGT GGTGCGCACC 1560 TGTGGTCCCA GCATTTGAGA AGCTGAGGTC GGAGGGTTGC TTGATCCTGG AAAGTCAGGG 1620 CTGCAGTGAG CCATACTCCA ACCTGGGTGA CAGAGCAAGA CTCTGTCTGT CTCTTTGGGA 1680 AAAAAAAAAA ATCCAACTTA CGAGTTCTCT TGTGCTCCCT CTCCACTGTT CCTCTTTGCT 1740 CTTTCATCCC TCCTGACTCC AGAAGAGGGC TCTACCACTC GCTGCTAATG CCTTCACATT 1800 TGTCTGGATT CCTGCCTCCT GGGGACCTCA TCCTTGCCAG CCCCTGTTGC TGTGCCTGTG 1860 CCCTACCAGG GGTGTTTTCA TGTTCTCATC AGTGACCCTG CTTAGCCCTG AATATCATCA 1920 GCCGGCTCAT GCCTGACTTC TCTGTGGAGG GATTCATCCC ACGTGCATTC TTCAGGGTAT 1980 GAATCCCACA GGACCAAGAC CTTCTGGATC CCTTTCCATT TCTTCACATT CAAGAATCTC 2040 TGCAAAAGAA TGTAGCCTAA CCCCCCTAAC AATCTAAAAC TTCTTCCCAA GCACCATTTA 2100 GTGCCCCAGG ACACTTGCCT GTGGCCAGAG CGACTCTCTT CCTTTCTGCC CTTTCCATTG 2160 TCTACCCCAC CTGCCTCCCC TTTGAAAGTT GTTCAGGTTT AACTTTCCCT CCCTATTCCC 2220 TTTGTTCCCG TTTGTAGGCA GGTCTCCCTC CCCTGCAATC CCATACCATG TTCAAACAGG 2280 TTTTCTTAAA ACTCTTACAT CACTTTTCTC AGCCTACACC CCCTACTGCC CCAGACCCAA 2340 CCCCAACTCT CCCACCTCCT GTAATTTGCC CACTCCACAC ACACCCTCTG TAATGAGGCC 2400 CCTGCCCTTC AGCAGGACCT GGCTCCTGGG CTTCTTGTGG TACTTCCTGG GTATCAGCTC 2460 CCTCCAGCCT CCACCTCCAT ACCCTTCCTC TTACACTACC CCAGTCCACT AATCTCTGCT 2520 TTTTCTAGAC CTAAAATTAG 2540
|