Tag | Content |
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EnhancerAtlas ID | HS082-19051 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr2:113835310-113837230 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GFI1 | MA0038.2 | chr2:113835969-113835981 | TGCTGTGATTTC | - | 6.22 | Gfi1b | MA0483.1 | chr2:113835969-113835980 | TGCTGTGATTT | - | 6.62 | TCF3 | MA0522.2 | chr2:113835575-113835585 | AGCAGGTGTT | - | 6.02 | ZNF263 | MA0528.1 | chr2:113835913-113835934 | CCCTCCCCTTCTCCCTCCCTG | - | 6.03 | ZNF263 | MA0528.1 | chr2:113835906-113835927 | ACCCCCTCCCTCCCCTTCTCC | - | 6.81 | ZNF263 | MA0528.1 | chr2:113835909-113835930 | CCCTCCCTCCCCTTCTCCCTC | - | 7.19 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26693 | chr2:113834343-113836231 | Esophagus | SE_26693 | chr2:113836267-113839903 | Esophagus |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 4 | Chromosome | Start | End |
chr2 | 113835950 | 113836479 | chr2 | 113836692 | 113837210 | chr2 | 113835949 | 113836406 | chr2 | 113835577 | 113835744 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I113076 | chr2 | 113834552 | 113838205 |
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Enhancer Sequence | TGGCTCTCGT CATGTTGCCC AGGCTGGTCT TGAACTCCTG GGCTCAGGTG ATCTTCCCAC 60 CTCAGCCACC CAAAGTGTTG GGATTACAGG TGTGAGCTGC TACATCTGGC CAATCACTTG 120 GTTCTTATGG GACATTCATC ATACTGTGTG AGAAGAGCTA TGGTACCAGG TAGAGACACC 180 ATTGTAGCCT AGAGGTGGAG CTGGCAGGGA GGGCTGGGCA GGGCTTCACA GAAGAAAGAG 240 CATATAATCT GGGCCTCAGA GAAAAAGCAG GTGTTTTCCA GGCAGAGAAC GCAGGGATGG 300 GCATCCCAGG CAGAAAAACT GCTCAGGAAG GTGTGATGAT GGAGAAGAGC TCCCAGCACA 360 TCTGAGGTGA GTCATCAATG TGGCTGGGAC CCAGGGCTTG GACTGAGGAG TGGCTGCAAA 420 TTCACATGAG AAGATGGGTG GCTCCTGATT GCTAATGCCT TGTGAAGGAG TTTTTATCTG 480 GGAGGCCCCA AGGAATCATC CAGGTATTTC AGGCAGGACC CAGATTTTAA TCCTGGGCCC 540 CTCAGATCAG CACTGGGCCA ACACAGATGC TACTGGGTCC TCAGCTCTTC TCAGCCACCC 600 CCTCCCTCCC CTTCTCCCTC CCTGACTTCT GTTTAGCACT GCCCCGGGGT CAGCTTCCAT 660 GCTGTGATTT CACAGTCAGC CTGACCCCTG CTTCATCTTC CCTGACCAGT TCATCACCTT 720 CATGCATGTG TTGAAAGACA AACTTTGGCA TATTAAAATT TTAAGGAGTT TATTTGAGCA 780 GAGAATGATT CATGAATCAC AAGGTGCCAA ATTGCAAGTG ATTCAGGGCT CCACCCAGGG 840 GCTACCGGAA AACCATTTAT AAGTTGTTCA GGAAGCAAAA GGAAGAAAAA AATTCATTGG 900 TTAAGTGGAA AATCCTTAGT TGCAGGTTAG TCGGCGGTTC CTGATTGGCT AAGCTTAAGT 960 TTCGTTTTCT TAGTCAATGA CCATTCACTC TGGGTTGGGT TTTAGTTTAC TTAGGCAGGA 1020 ACCCAACACG CTGGAGTCAT CTCAGCCTAA TACCTTCCCA ATTAATTATT TTAACACATG 1080 GTAACTCATT TCTGCTGGCC CTTCCCTTGT GAACTGTGCC CATGGACCAC CCAGGCAAAT 1140 GCAGGCCTCC TCCTACTTAC TAGTGGTGCT GTTCCAAGTT GAATCATGTT CTCTATATAA 1200 CTAAAAAAAA TTTTCACATG TAAAATATGC CAATTCTCTA ACAGTGCACA GAAGAGGAAG 1260 AGGACATAAA GACTTAGAAG ACATGTCTCT ATGACTGAAG GACACATAGT GCAGATGGGA 1320 AAACCAGACC TTGTGAATAA AAGCTCATAT TTATTGACTG CAAGACACTC CAAATAGCAC 1380 TTAGAATCAA ATTCTGCAGG ACTGTGGTAG AAATAGTGAT GGGACTTTCT GGCACTAGGG 1440 TTTAAAAGTA AGGAATGGAG GCAATTTCTG ACAGGTGCAG TTCAGCGATG CCAAGAGTAT 1500 TCTTCTCCCA CGCCCCAAGG CTCATTCCTT AAATTCCTTC TCCTCCCTAG AAACCACACC 1560 AAAGTCTTCA CTCCAAAACC TAACCAGGCT AGAGGGTTAT TATTATGTGA ATTCTAGGGA 1620 GAGGTACACT TTAGGTCTTA TCCACTATTT ACATCTCAGA ATGAACTGGT AGGTCCAGAG 1680 AGAGAGCAAA CAGGCAATTA AACACAGTGT GGCCAGCTTT CGGTCAGGTA GCACCAGGAG 1740 CAGGGTGGGT GGGGAGGGTG AATGTGTGTG TCTGTATGTG CATGACGTGT CCATGTATGT 1800 GTATGTGTGT GCTGTGTGTG CATACGTGCT TACAAGAGAC TCCAGATGTA GGCAGCAGTT 1860 GATTCACAGG GGGCCTAGTC TTTGTTCCAA GAAGCTATGG AACAACTTCA CACAAGAGGG 1920
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