Tag | Content |
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EnhancerAtlas ID | HS059-33588 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr3:156299410-156301160 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
STAT1 | MA0137.3 | chr3:156300974-156300985 | TTTCCTAGAAA | - | 6.14 | STAT3 | MA0144.2 | chr3:156300505-156300516 | TTTCTGGGAAG | + | 6.02 | Stat4 | MA0518.1 | chr3:156300971-156300985 | TTGTTTCCTAGAAA | - | 6.09 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_59616 | chr3:156280725-156398876 | Ly4 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | ATTTAAATTC AATAGAATAT TATACAATAA CCAAAAATGA ACAAGAGGGA AAAGAGGAGG 60 AGAAATGTTT ACTAAAATAT GCATAAACAA ATTCTATGAG TAACTTGATT ATAAATAGGT 120 ATGTTGGTCA GGCTTTGATC AGCATGACAT AAGGGCTACA GGAACTAGGG TAGCCATGTC 180 AGGGCCTAGA TTCTGAGACT TGTCCTTGCT AAAACTAACT CTCTGTCTCT CATATCTCCT 240 CTTCCATTTC TCATTGTTAC TTTTTTCTAC TTTACATAAG TCTCTTCCAT CACAGACAGA 300 CTTTCTCCTT AGAGATTAAG GGAGGATTAT GGCAGATAAT GGCTACCAGA ATTCACAAAT 360 CTGTGAGCCA GTCCTAAATT TTAAAAATCC CCCAGGGAGA CTCTGACAGG TCAGAATTGA 420 CACACAGCCC CACCTTAGAC CAATCACCAT ACTCATAGGA ATGGCTACCA GGAGTGGTCA 480 GACCTAGAAC AAGAGCCCTT TCCTGTCATC AGAGATGAGG GTACCATGAT TGACAGGCTC 540 ATCAGAATCA CCTGTTGGAG TGGAGAAGCA GTAGTTTCCC AAAGGAAATG TGTGTGTATT 600 GGAGTGGAAA GAGGGGAGCA GAAGATTAGA GCAGAAGCAG CCAAGGTGCT GAGCAGACAA 660 GAAAAACAAC AGTTGCATTC TACAAATTGG CATGCATGGC CATCTGTGAA TTACCCCTGC 720 CACTGCTACA GCCTCCTTTT TCATCACTCT GTACCTCTCA TCCTGTGTTA GGGATATTCT 780 GAACTAATTA GAGTTCTGTA ACTTCTGGGC TCCACCTTTG CACATGTTGT TCCTTCTTTC 840 TCTAAGCCTT CCTAGTCTTT CTGCCTCTAC CTCGCTAATT CCAACTCATA CTTCAGCTCA 900 TATTGCAGCT ATCACCTGCT CTAAGAAGCC TATGAGGATT CTATACTTGC CCCCACTCAG 960 AGTTTTAGAA TCCCACACGT GCTTATAGTG CTTGAAGCTT ACCTCTAGCA CAGCTCATAC 1020 CATGTCATAT TGTGATACAC TCCAGCTAGT TTAAGCAGAA CAGGACTATT ACAAGATCCA 1080 AGTTAGCTTA CAGAATTTCT GGGAAGCTGG GGAGCCAAGC TTGGGTATTA CTCGGACTGT 1140 GAGCAGTCAG GAGAAACATC CACAATGATG CAGAAACCCC ATGGCCAGCC ACTGCCTGCC 1200 ACTTAGCCAC TTCAATACTC CACCAGAATT TGAGAACTCC TGCAATCACT GTCCCTAGAG 1260 AACTGAGCAC CTCTACTGCC CTTCCGGCCA CCAGAAGAAC CTGTGGCCAC CAGCTCATAG 1320 TAGTTGCTTT CATCTTCCAA ATCTCTGCTT GGCAGAAGCT CGGTCATGTG AAGAATCTAG 1380 ATGCAAGGGA AACTGAGAAA TGTAGTCTTT TTCATGACAA ACAGAAGGTT GAGTCATTTT 1440 GAATGAGCCA ATTTCCCAGT CTTCCACCAA ACCTCCACAA CAACAAATTT GTTGTTAAGG 1500 GCAAACCAAT TTATGGTTGT CCTACTGTCT TGGTAAGTAG TTTCATTGTC TGTATAAGAT 1560 CTTGTTTCCT AGAAATACTT TTAATTTAAT ATCCATTTTT ATCTAGTACT AGTATTGCTA 1620 GGCCAGCTTT TTGTTGTTGT TGTTGTTGTC ACTAATTTTC TGGTATGTCT TTTTTCATGC 1680 CTTTATTTGT AATTTTTCTG TGTTATTTTG TTTGAGGTAC ATAACTTATA AACAGATATA 1740 TACCTGCATT 1750
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