Tag | Content |
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EnhancerAtlas ID | HS181-11032 |
Organism | Homo sapiens |
Tissue/cell | Sperm |
Coordinate | chr4:74976880-74978490 |
Target genes | |
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) |
NFYB | MA0502.1 | chr4:74977630-74977645 | CCATGGACCAATCAG | + | 6.98 | RREB1 | MA0073.1 | chr4:74977965-74977985 | ACACAACACACCCCCATCCT | + | 6.4 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_34020 | chr4:74973468-74984340 | HCC1954 | SE_34944 | chr4:74973434-74984043 | HeLa | SE_35924 | chr4:74973407-74984079 | HMEC | SE_38660 | chr4:74973379-74978167 | HUVEC | SE_46049 | chr4:74973285-74983971 | Osteoblasts | SE_55844 | chr4:74970769-74984442 | u87 | SE_64715 | chr4:74973303-74981674 | NHEK | SE_67651 | chr4:74970769-74984442 | u87 |
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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 |
GH04I074107 | chr4 | 74973459 | 74983803 |
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Enhancer Sequence | ATGACTTAAC TCTTTGTTCC AGGAAATTCT TACATAGAAA ATAAAACTAA GCTCATGGAG 60 AACTTTGCCA TTTGCTTGAG GAAATTCTTC TAAGTCAGTT TATTCAGGAC ATCAGTTTGC 120 ACATCTGAGC CAGCAGATCA CTCCTCAGAC AAGTTCGCTT TTTCTAGCAA GACCCTCACC 180 TGTTTTGTCC ACTAACTCTA TTATGTCAAC AACTGTGCCC AATTCCAGTC CATTCCCTAC 240 CTTGTCAGAT CAGTTTTAAA CATTTTGAGT CCAATTCTCT GAACATCCTC CTTCTGAGAC 300 ACTAAAATGC TGTCAGAGCA TTGTTCCTCC TGTTGAGTAA TTCTAATAAA TTTAACGTTT 360 CCTGATTGAA GGGGTTTTTT GTTGTTGTTG TTGGTAGTAT TTCTGATGAA TTGGCAGTTG 420 ATATGTTCTA TTGGAGACTA GAACATAAGA ATGGGGAAGG TGATACTTAT AATAATCTAT 480 CTGGGTATAG TTAGGATCTT CACATGCCAC ACTATGTAGT GACATAATTT GACCTGGAAA 540 TAGCTGGTCA CATTGGCTAT ATTGATAGCA ACAGGAGATA GACAAATTCT TAGGCAGACA 600 GGGATGCGTC CCTGGTAAAA CCTGATCTCC AAGCCAAAGA CAGCCTGAAG ACTGAAAACT 660 GAGCTGCCAG TTCGGGGTAG AGCCCATGAC CAGAGTGAGA ATTTCCTCGA TGCCTTTTAG 720 CCAATATAAT GATGCTTTTT CCAGGCCCAC CCATGGACCA ATCAGCATAC ACTCCCCCAT 780 TCTGAACCCA TAAAAACCCC AAACTCAGCC TTACAGACAG CCACCTGCTT TTGGGCCTCC 840 TCTCACACAG AGGACCATCC ACTTCAAGTC CCCTCTTGTG TTGAGAGCTT TTCTGCCACT 900 CAGGAAAATT CTTCTCTGCT TTGCTCACTC TCCGGTGTCT GTGTACGTCA TTCTTCTTGG 960 TCACAGGACA AGAACCCGGA ACATGCCAAA AGGGTGTAAC ACATACTCCT GCTCACTGAG 1020 TTACAGGAGT GAAAAAAACC ACTGGGTGCC GCATGCCCCT ATTTAGCAGG TACAAATGAG 1080 CTGTAACACA ACACACCCCC ATCCTCCAAG CTGCAGGCAG CAGGGAGAGC TGTAACATGC 1140 CTCCATCCTC CGAGCTGCAG GCTCAAAGAA GTGAAGCAGT TAGGCACTAT TCCCTCCTGG 1200 CCAGCTTGCT GAACTACAAA AGCTGCAACA TTTCTTGGGA GCTTAGACCT CAGGATTCCC 1260 CAGGCGAGAG CTGTAACATC ACCTGGGGCT CCACAGTTGC TGGCATCTCT GAGTTTTCAG 1320 GTGCCACTGC ATTCCCCTCA TCTAGACTCC GGCTCCCAAT GCAAAAGCTG CCTGTGGCAT 1380 GCCAAGTTTA GCCACAGGCA AAACACAGAG TCCCTGTTCA GATGTGGGAT CCAAGCAGGT 1440 AGCACAAGCT GAGTACAGCC CATCAGGCTG AGTGGGAAGA GTGAGCCCAG CAGGCCTTGG 1500 CAAGACTACA GGCAGAGGTC ACAGCAGCCA CAGAGATTTC CAGCTGGTGA AGCAGCACTG 1560 AAGGAGTCCT GTAACAGTAT GTTAGTCTAC AAACTTGGTA AATTCTCATT 1610
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