| Tag | Content |
|---|
EnhancerAtlas ID | HS060-32104 | Organism | Homo sapiens | Tissue/cell | GM12891 | Coordinate | chr7:99051890-99054050 | 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 | chr7:99053097-99053112 | CAGGTCACAAGGTCA | + | 6.49 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CAGTCTAGTT ACCATCCACT GTGGTGGGCT AGAGACTGTC CTATTTCCTA CCACACTGCA 60
CTGAGGCACG GTAAAGGATG GTGAGAACGC CTGCCTAGTG AATGGACGGG GCCTGCAGGC 120
AGGTGAGGGA AGCCCCCAAG AGGCCGGGAA CAAAATAGAA ACACTGATCC AGGGAAGGGT 180
GAGCCCTTGG AGCCGCTGGC TGTCCTGGGG GCATCCTTGG ATCCTGCAGG GCACACCCGA 240
GAAAACAGGA CACTGGGTTA CAGCACCCCT GTCCCCATCC CCTCCCCCAG TACATAAAAT 300
GGGACTCAGG AAGGGTGAGC TTCAAGAAAC CTCCTCGAAA ACTGTCCTGT TCACTCCTGG 360
CTCTGTGGGA AGCGGGGAAA GGGGAGGAAA ATCTCTTGAT AGTTTGACGT TATTAATGGG 420
CCCTTATGTG AGTCTAGGCC TGTATTCATG TCCTTGGTTA AGGCTGGAAA GTTACAAACT 480
AAGTTTTCTA ATCTAAAATC GCCCCAGGAT TGGTGTGTCC CTGGCACGTG GCAGGAGTAA 540
CCCCCAGTAC TCTTTGAAGA GTATGTTCTC AACCCAAGGC GCACACAATT CCTACAGCTG 600
GAGTTCTGAA GAATGAGTCC AGATTAAAAA TCACAAAACA GGCTGGGTGT GGTGGTGCAC 660
GCCTGTAGTC CCAGCTACTG GGGAGGCTTA GATGGGAGGA TTGCTTGGGC CCAGGAGGTC 720
AAGCCTGCAG TGAGCTATGA CTGCACCACT GCACTCCAGC CTGGGCAACA GACTGAGACT 780
CTTTGTCTCC AAAAAAATAA AAGAGCATGG AAGTGGGGCA CTGTGTAGAG CAGACTTAGC 840
TGTTATCTTG CCACCCTCCA GGCCTGTTAA GCGGGGCCAC TTCTGTGCAG CAAGCGCCCT 900
TAAGTCCTGG AGCCTTAGAA AGGTAGGGCT GACCGCCCCT GTCCACAGCC TGTCACCCCA 960
TTAATGTCAG AGACACTTCA TGTAAGTCCT GGATTCCCCA GAGTCAGCTG TGGGGTCCGA 1020
CAGACATGCC AGATGCCGTG AGCAGGGTGT GTGGTCCCTC CCCCAGCCAT CATGTTAGCC 1080
CTACAGCCCA TCGGCAGCCT CTCCATACAG AGTCACACCT GCAGATCAGA CAAAGTTGAA 1140
AACACAGGGA CAGCTGGGTG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT TGGGAGGCCG 1200
AGGGGAGCAG GTCACAAGGT CAGGAGTTCG AGACCATCCT GGCCAACATA GAAGAAAGAA 1260
AACAGGAATT GCAGAGCCAG GGAATAGAGC TGGCAAGAGT GTTGGGTGCC AACTGGGCAG 1320
AGCCCCTCAG GGCAGCAGGG ACTCAGGGGT GGGTGTCAGT ACAGAGTCAG TGCCCCCAGC 1380
TGCCTCCTGA CCCTTTTGTT CAGTGCTTGA GGCTGCCGTT TTAGGAGTCA TAGAGTAAAG 1440
AGAAGCTATG GAAGGGCCTG GATAATCAGG ACTGGGATGA GGCAGGGTCA GGGCTGGATT 1500
TGTCATGTGG CTCTGCAGGC TCCCCTTACC CAAGTCTAAG CATCGTCCCA TCTCTCTGAT 1560
CCTGTAATCA AAACCTGTCC CCAAGGTAGC TTAGGTGTGT CACAGCCACG AGGGAAAACG 1620
TTGGGTACAG CCCACCCTCT GTCCCCAGCA GTGGCTCCCC AAGGGAGGGG AGGCTGGGAC 1680
ACTTCTGATG CTGTTCCCTC CCATCTCCTG CCAGGGAACC CCAGACCTTG GCTCAGAGGT 1740
AAGTGACTGG CCTGTGGTGC AGAAGGGCTT GGTCCCCAGA CGGGGTGGCG GAGCTCAGGT 1800
GCCACGGGCT TCTCTTTGTC CTGCTACCCA CTTGGGAGTC CCTCCCTGGG CAGGCCATGT 1860
GTCCAGGTGG GAGAGTTGTG GGCCTGAAAG AGCAGGTCGC TAGCAGGTCG CCTTCTGGCG 1920
GCCTTGTTCT CCCTTGCATC TGCGGAGTTG CTGGCTAGTT TCTGCACCAC TGCACTTTCC 1980
ATCCTGAGCT CCCTCACCCT CTAATTTGAA AGAAACTCTG TACCACTGAG AATTTCAGAG 2040
TCATGTCCCG ACTGGGGACT TGGTGGATGA TTTGGGATTT GGTGGGCACT CCCTTAGTTG 2100
AAAACTGCAT TTGAACAGTG TTGTTGTCTG TCTCTCCTCT TCCCCCACTT CCTGCTGTTC 2160
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