| Tag | Content |
|---|
EnhancerAtlas ID | HS176-37977 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr7:99051760-99054050 | 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 | TGAGTCCCTG GGCTGGGGGA CAGGGTGGGG TCTTCCCTTA CCGTCAGTGG CCATTCCCTC 60
ATGCCCCATG TGTTTGGTGA AATGAGAAAA ATGAAAACAT TCATTTTTGC TGATTGTAAG 120
CATAAAGTTA CAGTCTAGTT ACCATCCACT GTGGTGGGCT AGAGACTGTC CTATTTCCTA 180
CCACACTGCA CTGAGGCACG GTAAAGGATG GTGAGAACGC CTGCCTAGTG AATGGACGGG 240
GCCTGCAGGC AGGTGAGGGA AGCCCCCAAG AGGCCGGGAA CAAAATAGAA ACACTGATCC 300
AGGGAAGGGT GAGCCCTTGG AGCCGCTGGC TGTCCTGGGG GCATCCTTGG ATCCTGCAGG 360
GCACACCCGA GAAAACAGGA CACTGGGTTA CAGCACCCCT GTCCCCATCC CCTCCCCCAG 420
TACATAAAAT GGGACTCAGG AAGGGTGAGC TTCAAGAAAC CTCCTCGAAA ACTGTCCTGT 480
TCACTCCTGG CTCTGTGGGA AGCGGGGAAA GGGGAGGAAA ATCTCTTGAT AGTTTGACGT 540
TATTAATGGG CCCTTATGTG AGTCTAGGCC TGTATTCATG TCCTTGGTTA AGGCTGGAAA 600
GTTACAAACT AAGTTTTCTA ATCTAAAATC GCCCCAGGAT TGGTGTGTCC CTGGCACGTG 660
GCAGGAGTAA CCCCCAGTAC TCTTTGAAGA GTATGTTCTC AACCCAAGGC GCACACAATT 720
CCTACAGCTG GAGTTCTGAA GAATGAGTCC AGATTAAAAA TCACAAAACA GGCTGGGTGT 780
GGTGGTGCAC GCCTGTAGTC CCAGCTACTG GGGAGGCTTA GATGGGAGGA TTGCTTGGGC 840
CCAGGAGGTC AAGCCTGCAG TGAGCTATGA CTGCACCACT GCACTCCAGC CTGGGCAACA 900
GACTGAGACT CTTTGTCTCC AAAAAAATAA AAGAGCATGG AAGTGGGGCA CTGTGTAGAG 960
CAGACTTAGC TGTTATCTTG CCACCCTCCA GGCCTGTTAA GCGGGGCCAC TTCTGTGCAG 1020
CAAGCGCCCT TAAGTCCTGG AGCCTTAGAA AGGTAGGGCT GACCGCCCCT GTCCACAGCC 1080
TGTCACCCCA TTAATGTCAG AGACACTTCA TGTAAGTCCT GGATTCCCCA GAGTCAGCTG 1140
TGGGGTCCGA CAGACATGCC AGATGCCGTG AGCAGGGTGT GTGGTCCCTC CCCCAGCCAT 1200
CATGTTAGCC CTACAGCCCA TCGGCAGCCT CTCCATACAG AGTCACACCT GCAGATCAGA 1260
CAAAGTTGAA AACACAGGGA CAGCTGGGTG CGGTGGCTCA CGCCTGTAAT CCCAGCACTT 1320
TGGGAGGCCG AGGGGAGCAG GTCACAAGGT CAGGAGTTCG AGACCATCCT GGCCAACATA 1380
GAAGAAAGAA AACAGGAATT GCAGAGCCAG GGAATAGAGC TGGCAAGAGT GTTGGGTGCC 1440
AACTGGGCAG AGCCCCTCAG GGCAGCAGGG ACTCAGGGGT GGGTGTCAGT ACAGAGTCAG 1500
TGCCCCCAGC TGCCTCCTGA CCCTTTTGTT CAGTGCTTGA GGCTGCCGTT TTAGGAGTCA 1560
TAGAGTAAAG AGAAGCTATG GAAGGGCCTG GATAATCAGG ACTGGGATGA GGCAGGGTCA 1620
GGGCTGGATT TGTCATGTGG CTCTGCAGGC TCCCCTTACC CAAGTCTAAG CATCGTCCCA 1680
TCTCTCTGAT CCTGTAATCA AAACCTGTCC CCAAGGTAGC TTAGGTGTGT CACAGCCACG 1740
AGGGAAAACG TTGGGTACAG CCCACCCTCT GTCCCCAGCA GTGGCTCCCC AAGGGAGGGG 1800
AGGCTGGGAC ACTTCTGATG CTGTTCCCTC CCATCTCCTG CCAGGGAACC CCAGACCTTG 1860
GCTCAGAGGT AAGTGACTGG CCTGTGGTGC AGAAGGGCTT GGTCCCCAGA CGGGGTGGCG 1920
GAGCTCAGGT GCCACGGGCT TCTCTTTGTC CTGCTACCCA CTTGGGAGTC CCTCCCTGGG 1980
CAGGCCATGT GTCCAGGTGG GAGAGTTGTG GGCCTGAAAG AGCAGGTCGC TAGCAGGTCG 2040
CCTTCTGGCG GCCTTGTTCT CCCTTGCATC TGCGGAGTTG CTGGCTAGTT TCTGCACCAC 2100
TGCACTTTCC ATCCTGAGCT CCCTCACCCT CTAATTTGAA AGAAACTCTG TACCACTGAG 2160
AATTTCAGAG TCATGTCCCG ACTGGGGACT TGGTGGATGA TTTGGGATTT GGTGGGCACT 2220
CCCTTAGTTG AAAACTGCAT TTGAACAGTG TTGTTGTCTG TCTCTCCTCT TCCCCCACTT 2280
CCTGCTGTTC 2290
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