| Tag | Content |
|---|
EnhancerAtlas ID | HS129-20270 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr2:111933210-111935370 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr2:111935287-111935302 | TGAACTCCTGACCTC | - | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr2:111935021-111935036 | TGGCCTCTTGACCTT | - | 6.65 | | RARA | MA0729.1 | chr2:111935284-111935302 | GCTTGAACTCCTGACCTC | - | 6.52 | | ZNF263 | MA0528.1 | chr2:111933375-111933396 | GGAGGAAGAGTGAATGGAGAG | + | 6.03 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GCTTTGGAGG AAGAGGAGGG AGGACTTCCT GATGTGGAAG GTGAGGGAAC AGAAGGAATC 60
AAGGATTCTA AAGGATGATT TGGGTCAGAG CAATTAGCGG GGATGGCGCT TCCTGAGAAT 120
AGAAGCAGGA GTGGGAAGTG AGATCGGTTG GGGAGGGGCT GGGGTGGAGG AAGAGTGAAT 180
GGAGAGTTCT GTTTTGCTGG ACCACGAACT CAACTCAGGG GTTATCTAGA AACAAAGGGC 240
TGTCAATTCA TTTTAAAGGG CTTTTTTTTA AGTTGAGTTT CTGGAAAGAA ACTCCAGGAA 300
GGTGGACTGT ACCCACTGGC TGCTTAGAGA AAGCCTGGAG CATGAATATT TAGACATTTG 360
CTTTAATGAA GCACTCTCAT AAGCCGGGGA AACAGGGCCT TGAGCATCTG TTCATGAGAG 420
GTGGATGATG GCCCAGTGGC GCCTATGGAG CATCTATGAA CACAGGCCAG ACAGGGCACA 480
GGAGGGAGGT CCTCAAGCCT AGAGGATGTT AGACTCCCCC AGGGGCTTTT ACAAAATACC 540
CATACCAGAG GCCCACCTCT CTGAGTCTGT GGTGGGGGTG CAGTGTCATA TTTTTAAAGG 600
GTCCCTAAAT GACTCCAGTG TGCAGCTGGG CTTGGGAGCT GCTGAATGAC AGCTTGCTCA 660
AAACTGCCAG GGATGACTCC AGCAGTGGTG GGGCAGCCAC AGCAGCATCG GGTCCAGCAA 720
TGCTCCCCAG GGACAATGCT CTGAAGGACA GCAATCAGCA AGGTGCTTTC TGTCTGTTTA 780
AATTTCTGTT GTAGTTGCAA AATGATCAAT TCTCTTTTCT GTTTCCCTTT GCCAGTTTGC 840
CCTGGCACAG GCATCCATGC CTCCAGCCAA ATTCAAGGTG AGTGGAGGAC AGAGTGTGCT 900
GTAGGGCCCA AGGCCAAGGC CAAGGCCACG GCAGGGTGGA GGTGAGGTGG CCCCGGGTTG 960
TGAGCCTGGG GAGAGCCCAG TCATCATCAG GTGAGTCAGA GCCTTCAACT GACAAACCCA 1020
AAGAACTCAG CGAGCTCAGA GACGGGAGGC GGAGCCATAG TGTGGACCCC AGAAGGGCTA 1080
GAGGTAGAAC CGAATCTGTG TGTGGCACAG GCAGTGAACG TGGGTGGATC ATGCTGTGCT 1140
TGAGCCTGGC CTTCCATAGC TCAGGAGAGT GTAGAGTGTG AGGGGAATCT CATAATCATG 1200
GGAAAAGTGT CATCATCGTC CCCTGAAAAA CAAGGACAGG AGGACACACA GGGGCAGGCT 1260
CTGAGAGAGC ACATTCAGGT GTGAGCACTT AGAAGGGAAA ATGATGATTT GTGTTGGGGA 1320
ACAGACCACA ATGCACATTG CACCCGGTTA GACACCAAGC TCTTCCAGGG GAACTTCTAC 1380
TTCTGATTGC TCAATACTAT GCAGAAATGG CCTCCGTGGG AGCCTCCACA GGCACACCCT 1440
TGCCCGCTCC AAGTCCCTCC CAGGACCAGA CTCTCTGTCC CTGCCCCAGC CAGCAAGGCT 1500
CAGAACAGTG GCTGCTCCCA GGTAACTCCC AGCCTGATTC CGGGTCCAGT CACCAAGCTC 1560
TGGGGATGGC CTTCTGATGG CTTATAGGTA AATGCTCTCA TCCCTGCTGG AAGATCCTAA 1620
TAACATTTTA AATTGTGTCT CTCTGTCTGT GGGGCTGCTA GCATTAGCCA GTGTGCCTCT 1680
GACTCAGCGG GATCTCGCCG TACCTGGCAC CTAGTAGGCA CTCAACACAC CGTTGTTGGA 1740
TGGGTGTGTG GCAACTAAAT GTCTGACGAG GACTCAGGTA AATCATCTTC TATGAAAGCC 1800
CAGTCTTTTC TTGGCCTCTT GACCTTCATC ATATGTATGT ACTGTTTGCA CTTTCTTTTT 1860
TTTCTTTTTT CTTTTTTTTT TGAGACAGAG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG 1920
TGGTGCGATC TCGGCTCACT GCAATCTCCA CTTCTCAGGT TCAAGCAATT CTCCTGCCTC 1980
AGCCTCCTGA GTAGCTAGGA TTACAGGCGT GCGCCAGCAC ACCTGACTAA TTTTTGTATT 2040
TTTAGTAGAG ACTGGGTTTC ATCATGTTGG TCAGGCTTGA ACTCCTGACC TCATGATCTG 2100
CCCACCTTGG CCTCCCAAAG TGCTGGGATT ACAGATGTGA ACCACCGCGC CTGGCCTGTT 2160
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