Tag | Content |
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EnhancerAtlas ID | HS107-00921 |
Organism | Homo sapiens |
Tissue/cell | Jurkat |
Coordinate | chr1:94157600-94158810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr1:94158160-94158181 | GACGAGAAAATGAAAGCACAA | - | 6.54 |
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| Number of super-enhancer constituents: 11 | ID | Coordinate | Tissue/cell |
SE_02579 | chr1:94157835-94160151 | Astrocytes | SE_34666 | chr1:94156170-94161986 | HeLa | SE_35914 | chr1:94156301-94161880 | HMEC | SE_37201 | chr1:94157138-94160168 | HSMMtube | SE_38161 | chr1:94157782-94160479 | HUVEC | SE_51729 | chr1:94156945-94160739 | Skeletal_Muscle_Myoblast | SE_57679 | chr1:94157517-94158002 | VACO_503 | SE_57679 | chr1:94158132-94159107 | VACO_503 | SE_59776 | chr1:94145101-94182733 | Ly4 | SE_63513 | chr1:94156834-94160739 | HSMM | SE_64440 | chr1:94157271-94160872 | NHEK |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I093691 | chr1 | 94156587 | 94162086 |
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Enhancer Sequence | TGAGTGAAAG TGGTGCTATG ATAAAGACAA TCTAGGGTTG GCCAGTTTGA TTTTTAAATA 60 AGTGATTTAT AACTGACACT GCATCATTAG GAATGAAGTG CTCGCCGCAC AGCTCGGCAT 120 CCAGTGCAAG AGCAGCTGGC ACAGCAAGCT GGAGGGCTGC AAGAGGCTGT CAGTTTGGCC 180 CTTTCCTCTC TGGTTCCTTC CTCACAGGAA CCCCCCTCCC CAGTGCACAC ACAGCTGCTG 240 TGGGGCACTG CTTTTGCCTC CTCTTGTGTG GTAACCATTT GGAACTGCTT TTAATGGTGC 300 TGTCGACAGT ACTGAGGTTT CCAAATGGTA AGAATAATTT CCAGATAGTA ACACAGTCAA 360 GCATAAGGAG ACACACAAGA ATTGGCCTAG GTGTCTGCAA AGAGGGAGAG AGCACCAAAG 420 GTTCTGATGG GGGAAACACA AACTAAATAT GAATCATAAA AGCTATGCTT ACCAGCCCAG 480 GGCTAAGAAC TTTGTGTGCA TCATCTGAGT TAATCCTTTC AGCAACCTAG AGAGGTGGGG 540 GTTATTAAGC CCTTTTTATA GACGAGAAAA TGAAAGCACA AAAAGGCAGA GTAACCAGCC 600 AAGTTCACAG AGCTGGGATG TGGAGCTCCC TAAACTGGCC TCCCTGACTC CACTGCCCAC 660 TTCATCTCCC AGTGTGAACC CTTGTTCCTC AGAGTGAGTG GGAGAGTTTG GGGTTGATTG 720 CTTGAGCGTG GTGTGGAATG GCACAGTGAA TCTTAAGAGA AGCAAGCAAG CTGGGTTAGG 780 TAAACTTAGC CCAGTGCCTG GCACTTGCTA GGCATTCCAT AGATATTTGA GATTTGGACT 840 TTTGAACAGA GTTTCAGACA TAGGGTCAGA GTGTGTGGGG GTCTCAAGCA GGTCAGGAAC 900 CACAGTCAAG CCTCTACATA CACTTGAATT TTCCCCATGG CAGGAACCCA CATTGAAGGT 960 TCACAGGTGT GTCCTAGCGC CGTCCTGGGG CTGTGGAGCA GCTGCCTCTC CAGTGCCCGG 1020 GGTTTGCCAT AAATGCCGAA TCTCAGCCCC ACCCTAAGGC ACTGACTCAG AACCCACATT 1080 TTAACAAGCC TCCCAGTGAC CTGTGTGAGA GGCACTGCTC CAACTCAACA ACCCTCCTGC 1140 AAGGGAGCAA GCCAGCAGTC ATCCTTCTAC CCAGTACAGG GGAAATTTCT TTTTCCTGTA 1200 CTAGGCTTAG 1210
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