| Tag | Content |
|---|
EnhancerAtlas ID | HS176-26136 | Organism | Homo sapiens | Tissue/cell | SK-N-SH | Coordinate | chr3:50418560-50421040 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| LMX1B | MA0703.2 | chr3:50420483-50420494 | GATTTAATTAA | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GGGGGAAGCG GGGAGCTGGG GTGGGGAGCA CCTGGGCTGT GTCCTGTCGA ACCCACCACC 60
ACGACACTCA TGCCTGTGCC CCCATTTAGA ATCCCCCAAC TGTTCTCGGC CTATCCAGGC 120
CCTCCCTATT TCCTAGGGCC CAGCTGGGGC TGCCCCAGCT CCTCCAGGAA GACTTTCTGA 180
TCCTCACCCC TCCCAAGCTG TGAAAGGAAC AGTTCAGCCT ACTCTTCCTC CAGGTCCCAC 240
ATGAGCAGGC AGGGCAGCTG TGGCTGGTAG CCTCTGGAGA GGGGCTGCCC AGGTGGCTGG 300
GTGCTGGGAA CTCGGAGCCC TCAGTCCAGC ATGCTGCCTG GAGCTAGCAC TGGTCCCCCA 360
GGAGCTCACC CATTCAGCAT GCACTCCAGG CTTCAGCCAC AAGAAAGCAA TTAAGGGCCT 420
GCTGATGGGG CTGGAATTAT TCAGCTATTA AGTTACCTGA TAAGCTGGAA GCCACTCAGC 480
TCCATGATTA ATCAACTGGG GCCAGAAGCA AGCAGGGGTG GGGGCGGGGG CTCTTGGAGG 540
GGCAGGGGCA TGCCAGATCC TGCTTCAACA CAGGCAAGTG TACTTGTACA CGCATGCGCA 600
CACTGCACAC CCCCCAACAG GTATACCTGT GTCTAACCTG TGTGTTTCCA GCCAGATGGA 660
ACCCACCTGC CTAGCACCCC AGCTGCCACC ATGGGCACAA GGGCACACAC GTTCATGCCT 720
ACACACCACT CTGCACCTAC AGGGGACACT CATGGGTCCT GCTCACAACC CCCTACCATC 780
AGTTACCCCA TTCTCCCTTC CCCCCAACCC TTGTAGTTGC ACGTGTGTGA TCCCCTGTCC 840
AGATCTATCC CTACACACAC ACACACACAC ACACACACAC ACACACACAC ACAAACAAGG 900
CTCCTCTCAG AGAATGGACT CCAATCCTGC GGACCCTTCA ACCTGGGCAG AGATCCAGGA 960
TGGTTTGAGC AGTACCCTCG ACCCCCAACT CGGGGCGGCC TGATGTGTGT GTGTGACACA 1020
TGTTCTCATG TGTGCAGTGA CCCTGTCCCT GGACACTAGG ACAAAACGGC AGGAGTGGGA 1080
CACAGCTGCT TCTGCCAGGC CTCTGTGCCT CCTTCCTCCT TCAGGGACCC CCACCCTCTT 1140
TCTTCCCATG TGGAGCCCAG CCACCGTCAC CCCGTACAGG GATCCCCATC AAAAATCTAC 1200
CTCAAGTGAG CACCAGAGAC CACCTGCAGC AGGCAGACAA AGGTAGAAAG CATGATTTAC 1260
AGTTCTCTAG CCTCTGCTCC GGCCCTGGGG CACTGACACA CTCTGGGGCA CTCTCCCTCG 1320
GGCGGCCCCT CTGGAGCGTG GAGCCTCTGC TGCGTCCGCT GCCTGATCCC TGCCCCCTGC 1380
TCCCACTCCC TTCGCTGTCT GTTCCTGTGG CTTCCCGTAA CTGACCATAA TGTGAAAACA 1440
AAACACATTT CAAGCATTGG CTCTGCTTAT TGAACAGTAT GTTATGGTCC TGTTCCTAAT 1500
TTAGAAACTT AGTGAGTTGA ACAATTTCTA TTTTTCTCTC TAAGGAAAAA ATAAAGCCAG 1560
GCCCTCCAGA GTTTCACACA GTACTGTTTG CCCTGAGAGA GTCTGCCTGG CAGGTCCCAC 1620
CCCTCACTGT GTCTCGGTTT TCCCATCTGC ATAATGACAG GCTTAGAGCA GAGGGGTGTC 1680
CCTGGTCCAG GTCAAGGGCC AAGAGGAGAC CCCTGCTCTG CGTGGGCTGT CCATGCAGGT 1740
ACCTGTGACC CCACACGCGC TTACCCATAC ACGGCAAGGC ACACTCGCGC AAACACCCCT 1800
GCGCCCGCCT GGAAAGGGCC TGCTACTCAG CCCCATGCGC ACAGACCCGT ACCCACCTGC 1860
ACATACTCTC AGATCATGCT GAGTTGGGAA AGGGGACCAT GCCCCCTTAG GCAGGTGATT 1920
ACAGATTTAA TTAAAAGTGA CACAGTAAAT AAAAAACATA TAAAATGCAA TTTATGTGGG 1980
TAGCGAGGGG TGACTGGAGA GGGCGGTGTG GCTCCTGTTT TAATTAGTGT GCCTGCCTGT 2040
GATAGTGCCC CTCGACTGGC TCGGGCAGGT GGCCTGCGGG CAGCCTGTGG GGAGCAGGGG 2100
GGAGCATCCT TCCCCACCCT GGCCTGAGGC TGCCCAGAGG GCCTAGCTGA CCCCGAGATG 2160
GAGAGGGCCT CCCTGAGGAC CCTGGGAATT CCCTGCATTA TGGAGCTGAG GCAGTGGCTC 2220
TGGGGCTTTT GAGTCCCAGC CCAGTGGGCT CCTTGGATTC CAAGGCTACT CTGTAGGTGC 2280
CCATAGAACT GTGTCAGAAA CAACAGGCCT CAGTGCCTTC AATCCTGCTG CTGGAGCTCC 2340
CCATCCAGTG TTTGACTCTT GGTTTCCTCC TCCTTTACCT CCCAGGAGCT TCAGGAAGTT 2400
CCTCCTCATG TCTGACTCAA ATCCTTCTAG CTATAGTGAC CTCGTTTCCC CATTGTGTAA 2460
AGCTGCCTTG TCCCTGAAGC 2480
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