Tag | Content |
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EnhancerAtlas ID | HS062-15632 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr8:28268070-28270850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr8:28270347-28270358 | CATGAGTCACC | - | 6.62 | IRF1 | MA0050.2 | chr8:28270023-28270044 | TCTTTCTTTCGTTTTCTTTTT | + | 7.04 | JUND | MA0491.1 | chr8:28270347-28270358 | CATGAGTCACC | - | 6.02 | Nr2f6(var.2) | MA0728.1 | chr8:28268515-28268530 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF740 | MA0753.2 | chr8:28269019-28269032 | GTGGGGGGGGCTA | - | 6.19 |
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| Number of super-enhancer constituents: 30 | ID | Coordinate | Tissue/cell |
SE_00229 | chr8:28267815-28271002 | Adipose_Nuclei | SE_09976 | chr8:28268647-28270464 | CD14 | SE_10881 | chr8:28255172-28272037 | CD20 | SE_14002 | chr8:28268202-28269750 | CD34_Primary_RO01536 | SE_17678 | chr8:28268442-28270830 | CD4p_CD25-_CD45RAp_Naive | SE_24655 | chr8:28268237-28268549 | Colon_Crypt_2 | SE_24655 | chr8:28268938-28270290 | Colon_Crypt_2 | SE_26645 | chr8:28268002-28268679 | Esophagus | SE_26645 | chr8:28268835-28270881 | Esophagus | SE_27701 | chr8:28268034-28270348 | Fetal_Intestine | SE_28577 | chr8:28267958-28270431 | Fetal_Intestine_Large | SE_30513 | chr8:28268491-28270622 | Fetal_Muscle | SE_31606 | chr8:28268029-28268717 | Gastric | SE_31606 | chr8:28268836-28270741 | Gastric | SE_36706 | chr8:28268880-28270416 | HMEC | SE_40988 | chr8:28268744-28270549 | Left_Ventricle | SE_42550 | chr8:28268073-28268772 | Lung | SE_42550 | chr8:28268843-28270531 | Lung | SE_48797 | chr8:28268837-28270648 | Right_Atrium | SE_50770 | chr8:28268837-28270776 | Sigmoid_Colon | SE_52497 | chr8:28268072-28268725 | Small_Intestine | SE_52497 | chr8:28268749-28270511 | Small_Intestine | SE_53710 | chr8:28268789-28270686 | Spleen | SE_55734 | chr8:28268039-28270722 | u87 | SE_58644 | chr8:28219872-28277477 | Ly1 | SE_59813 | chr8:28219869-28277603 | Ly4 | SE_61002 | chr8:28174118-28277761 | HBL1 | SE_61739 | chr8:28219999-28279573 | Toledo | SE_62508 | chr8:28220381-28270893 | Tonsil | SE_67509 | chr8:28268039-28270722 | u87 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr8 | 28269888 | 28270200 | chr8 | 28270200 | 28270253 | chr8 | 28269269 | 28269540 | chr8 | 28269273 | 28269920 |
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| Number: 1 | ID | Chromosome | Start | End |
GH08I028410 | chr8 | 28267982 | 28270817 |
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Enhancer Sequence | GGTGTGGTGG TGCCTGCGGT CCCAGCTAGC TACTTGGGAG ACTGAGGCTG AAGGATCTCT 60 TGAGCCCAGG AGGTCAAGGC TGCAGTGAGC TGTGATTGCG CCATTGCAAT CCAACCTGAG 120 TGACAGAGCA AGACTCTGTC TCAAAACAAA ACAAAACAAA ACAAAAAGGA GCAACCATTC 180 TGAGAAGCCA AGGGTCAGAA GCCTGGGCTT GGCCTGCAGG CGATGATATG TTATCTGCTC 240 CCATAAGCGA CAGGAGCTGG CTCTGAAGCT AGAACCGAAG AAACAGCCAG TGACCAGAGG 300 CTGCTTGTTC TACAAGAAAG AGCACTGTCC TAGCCTTGGG GACGCAACTA GCAGAGTGAC 360 CAGAGCAAAC CATCCATAAA ATTATGACCA GGCCAGGCGC AGTGGCTCAG GCCTGTAATC 420 CCAGGCTGAG GCAGGCGGAT CACTTGAGGT CAGGAGTTCA GGATCAGCCT GGCCAACATG 480 GTGAAACCCC GTCTCTACTA GGCATAGTGG CACACGCCTG TAGTCCCAGC TACTTGGGAG 540 GCTGAGGCAG GAGAATCACT TGAACCCCAG GGAGGGGGCA GAGATTGGGC CACTGCCCAA 600 TTTTATATAT ATATAAAACT AGACAGTGGA TAGAAAACCC TATCTTAAAA AAAAAAAAAA 660 GAACTTTAAA AGTATTTGTA TCCTTTGATC CTTTAAAAAA ATGAAAATGA TTACATTTTG 720 GTACAGCTGT ACAATGTTAA CATCGAACCA TTAAACATAT TTATGATGTG TTTAAGGAAA 780 TGGGAAATGT TTCTAAGATA TTAAGTACAA AAAGCAAGAC ACTAATGACT TGCACAGAAT 840 GATCAAGTCT GTAAAGAGAA ATAGAGCAAA ACGTGAAGAA ATATCCCACT ACGTAAAGTG 900 TTTGCTTCGG GTGGTGGAAT TATGGGTGCG TTTCTGCGGG GTTTTTTTTG TGGGGGGGGC 960 TAATTATTTA CACTTTTCTG ATTTGCCATA GTGTATACAC TAAGCACATA TTACTTTTAT 1020 TATAAAGCGG CGGGAGGAGG TTGAAAACGA TCTCCAATCT CCTCGGTTTC CTTCCCAATC 1080 CTTTGCATCA GGTTGATTTC CTCCAGGCCC CTTCCTGAAA GTTCTGCAGG TGACGCAGCC 1140 CCGCGCCGGC CGCCGCCGGG AAGATTCGAG AGGCCATCGG CCAGGGAGCG GCGGCGTCGG 1200 GTTTCCGCGC TGCTCCCCCC ACTGCGAGTG CGGACGAGGA TGCCGGGCCG CGTCTGTCCT 1260 GCGGCTCGCT GGGGCCCGGC AGCCCCTCTG CAGCGCGGTG CGAGTTCCTG GAAAGGCTGC 1320 GTTTGCGCTC CCCGGCCCTG CCCTCGAGGC GGGGACAACC CGCGGCTTCA GCCCGGCGTC 1380 CCCCTCCTGC TCGGTCCTCA ACCCCGGCTG CGGCCGGCGG AAGCGCCCGG GCCTGGGAGG 1440 GAGAGGGAGG CACCTCCCTG CCGGCTCAAC CCCCTGGGCA AGGGGCCGGG AGGGCGCGGC 1500 TGGGACGTGC CCGGGCCCAC GAAGGCCTCC GCCCCACCCC TGCGCGCCGC CTGCAGGGGA 1560 GACCGGGCAG GGCGCCCCCC GCCTCCCAGG CCGCTCGCTG CAGGCTGCCG GCCGTGCGCA 1620 GGGGACCAGG CAAGGGGGCA GGCCATGCCT GCGGCCGCAA CGCTCGGGTC TCGCTGCCGG 1680 CGGCTGGACC GGCCCCTTTG TCCCGTAGTC CTGCTCCGCC GGGGATCCTG GGGAGCCAAA 1740 CCGAGCGCGC GCGCTGGCAT CTGTGTGGAC AGCGGGGGAG GCTGCCCGGT CTGATCCGTT 1800 GGCGCGCGCC CTGGCACGGC GTCCCCACGG CCTCTCCGGG GCCCGATCCC CGGCAGGCCT 1860 GAGCACTGAG CACTGCACCC GCTTTTCTTT GGGCGCGTGG CTCGTCCTCG GCCTGCTGCG 1920 GCCCCCTCCT TGCCCTGGCT TTGTTTTTCT TTTTCTTTCT TTCGTTTTCT TTTTCTTTTC 1980 TTTTCTTTTT TTTTTTTTTT TTTTTTTTTT TTGAGACAGG GTGCTGTGTG GCCCAGGCTG 2040 GGGGGCGGTG GCGTGACTAC GGCTCACTGC AGCCCTAAGC TCCCAGGTTC AAGCGATCCA 2100 GCTGCCCCAG CCTCCTGAGT AGCTGGGACT CACATGCGCG CCACCACACC CAACTAATTT 2160 TTGAAAAATC TTTTTTTAGA GACAGGTTCC TGCTATGGGG CTTGCCCAAG CTGGTCTTGA 2220 ACTCCTGGGC TCAAGCGATC CTCCTGCCTC AGCCTCCTAA AGGGCTGGGA TTACAGGCAT 2280 GAGTCACCGC GCCCGGCCAA CCCCACTGTT TTTCTACCTC AGCTTCTTTG TCTAAGTCTG 2340 ATCCACCAAA GGCCTTGGGC CCATCTTTCA CCTCCATCTG TAAACCCATC CCTGCCAGCC 2400 CCGCACTCTG CCCTGCAGAC ACACATGCCC GAGGCGAAAT CCAAGTTTAC TTCCACTTTG 2460 ACGGTAGGAC AAGATCCTGC CCTCTCATTG TCACCCCAAA ATATTCCCAA AGGCAAGAAG 2520 AGTTGACTCT TGCTCTATTA CCCTGGGCCC GCTGCTGCGT AATTTGCAGG GCCCAGTGAA 2580 AAATGAAATT GAGCAGAGAC GGAGCCACTG CATTCCAGCC TGGGTAAGAG AGCTAGACGC 2640 TGTCTCAAAT AGAGACAGGG TCTCACTCTG TCGCCCAGGC TGGAGTGTGG TAGCATGATT 2700 GTGGCTCACT GCAGCCTCTA CCTCCCATGC TCAAGAGATT CTCCTACCTC AGCCTCCCGA 2760 GTAGCTGGGA TGACAGGTGT 2780
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