Tag | Content |
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EnhancerAtlas ID | HS146-11460 |
Organism | Homo sapiens |
Tissue/cell | NHDF |
Coordinate | chr4:170258570-170259700 |
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) |
LMX1B | MA0703.2 | chr4:170258590-170258601 | AATTTAATTAA | + | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr4 | 170258712 | 170259094 | chr4 | 170259476 | 170259663 |
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| Number: 1 | ID | Chromosome | Start | End |
GH04I169336 | chr4 | 170258000 | 170259837 |
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Enhancer Sequence | ATTCAAATAG TCTTATGCAG AATTTAATTA ACAAGACTTG AAGCAACACA ATGTGGCCTA 60 TTTACATTGT GGAACTCAAT CATATCCCCC AGAGTCCCAG CCTCAAGTTG AAACCAATCC 120 TATAAACCAT CATGGTCTAA CTTGGAAATC CAACTAGCTT GCTCTTTGTG TTTTGACTTT 180 TCCACTTGGC TTGAGGTATT ATTCCAGATA CAGCAGGATG TATTAGCACA AGGAGGAAGT 240 CTTGGGCAAT TCAATCATTC CTAACAATCC TGGCCAGTGA ATTGAAGCTA TCTGAATGCC 300 TCACAGGGCT GAGGTTTGTT TTCCCAAAAT ACTCAAAGCT CTTTTATGAC TATACTTAAG 360 GGGTATGTGA CTATGTTTCC AGAAGAGAGG CAAGTTAATG TCTGGCTTCC ACATAAGAAT 420 TACAGTTTCT GAGATGCACA TGGTGCCCTA GGGAAGAGAT GTTTGCAATT GCCGATGCCA 480 CTCAAGGAGG ACCTGCATTC GTTGGGGACC ATGGTTCATG ATGCTGCAAA TATATTCTCC 540 TGGTTGGCTG GTTGGCATTA GGGTTTTCCA CAAAGAACAG TTGAATCTAA TCCTTCTTTG 600 TGGAGGAACT ACCTGATAGC AGTGAGTCTA ACCTGACCTT TTTGTCCATG CCACCAGCTG 660 GTGGCATTTG TTTGTTCTGG GCGATGATTG AGTGATACCT ACAAGAAAGG GAGGGGCAAA 720 GACATCTAGA GGTCTTGGCA AGTGTGTTGA ATGGGGTGGC AAGAACAAGT GTGTTGAATG 780 GGGTGGCAAG AACTGGGGCT ATCCCCTGCT GCTTCTGTTA AACTTCTTGG TAAGATTAAC 840 ACGAATGGAA ATCAAGTCCT GGTGATAATT ATCTGGCAGA GGATGGCAGG CCCAGTAGTT 900 AGTTAAAGGC AAGGCACTTA GTGCATTGGA GTGTTTTCTT TCCTGGGGAA GATCTCAGGG 960 TATCTTCCCA CCCTCATACT TTCTGGGGTT GGAGGAACTC TCTCCCCAGC TCTCACCACC 1020 AGAGAATCAT TGTGTTCATT CCAGTGGTTA CTCATCTCCT ACTTCACCCA CATCTTCGTC 1080 TAGATAAATT AGGTGCAAGA GGGATAAAGG CATATTTTAA AACTTTTATT 1130
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