Tag | Content |
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EnhancerAtlas ID | HS176-14640 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr16:316120-318290 |
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) |
INSM1 | MA0155.1 | chr16:316874-316886 | TGCCCCCTGACA | - | 6.92 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_53171 | chr16:315091-320078 | Small_Intestine |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 318039 | 318203 | chr16 | 316676 | 316852 | chr16 | 316980 | 317092 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I000265 | chr16 | 315301 | 316246 |
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Enhancer Sequence | CGTGTGTGCG TCTGCCTGTC TGTCTGCTCC CTAAGTAGTC AAATGGATTT GTTCCTGGAG 60 GAGTGACCAG GAATTTGCTG GCCAGCCTGG GTCAGGGTGG GGAGGGCTGC CGAGGAGGCG 120 AGCACCCCCA CCCAGACCTG CTCAGTCAGA AACTGGGCAC CCAGCAATCT TGACATCCTC 180 TGGGGGTCTC CGGTTTGAGG ACCCCTGCCC ACCAAGCTGG GCACCCTGGC CCCATGCAAG 240 CGGGTGTGCT CCCACCTGGA ACAGACGGTG GCCTCGGCAC CGCGTGACGT CTGAGGGCTG 300 GCTGGAGTCC AGCGTGAAGG GATGATGGTA GGGCCGGGGT GAGCTCTGGT GACCCTGCAG 360 GCAAGAGGAG CCCAGGCAGG GGCTTCCCGG AGATGCAGCT TTGGGTGTGG CGGCAGTGAG 420 GGGCAGGCAG GTGCTTTAGA GAGCCCTGCA GGACTGTCCC ACGGCCATGT ATGCAAGTGT 480 GAAAAGCCCC GCTTCAGAGC CACACAGGTG TAACCTTGTT CCCATTGCTC CTTCCAAGGC 540 GTGGTAGGGG GACGTGGGGG ATGAGGTTGA ACAGGTGGGT GCCCTCGTGC CAGGAAGCGG 600 TTCTCTTGTC CCTGAGAAAA GTAACTCAGC CCAGAAGGCC TTGGGTATGA AAGGGCCATA 660 TAGGGCTCTG CGGACGCGTC CTATAAGTGA GAACCGCCAG GCGGGCAGGG TGGGGCTGGA 720 GGGAGAAGGG AAGGTTCACT GGGGTTGCAA GAGCTGCCCC CTGACAGCAC GGGAGGGAGG 780 GCAGGGGGTC CCCAAAGGGA GGGGTCACCC TGCAGGTCAG AGGAGCAGCT GTGCCCCTGG 840 CCATGGAGGG GTGGGCAGGG CCATGAGCCC CACCCTGAGA AGCCGGAGTT GAGGGGCTGG 900 GCCAAGGGGT GCCATTGCTG GTGGGCAGAA GTTTCCCTCC CTGCAGGAAC AGCCTGCACC 960 CCCAGACTGT GAAGAAGGGA TTCTTGCCCT GTGGTCACTG CGGGCCCTAG AGAGTCTGGG 1020 CCATGCCATG CCATGCCCTC TGCAGCTCTG TGGCCTTAGG GCAGGCTGGG GACAACTGCC 1080 CCTCCCCAGA GGCTTCCTTA ACAGTTTCCT CACTGTTCCC CCTCTGGAGG GCAGGCGTCC 1140 CCACACACTA CCCTGCTCAC CCTAGCCCAC CAGAGCACAG TGCCCTGGCT GTCTCCTCCC 1200 AAAGACCAGA TGCCCCAAGT CTGCTGCCTG GGTCTGAGAG GGTCAAGTCC CTCCTCCACC 1260 ATCGACTCCA CACACCTGGG ACCTGCCCCC TCCCTCACCA CACACTGCAC ACATCACATG 1320 CACAATACAT TCACACATAT GTACTATACA TGTGCACACC TCATACATGC AATGTGCACC 1380 ACACATGCAT CCTACACGAC ACGTGCACAC ACACCACACA TGCATGCCTC ACAGTACACC 1440 TGCACACGTG CACTACACAC AATCACACGT GCTATGCGTA CACACCACAC GTGTGCCTCA 1500 GTGCTACACA TGCCTCATAC GACACGTGCA CACACATATG CATGCCTCAC AGTACACCTG 1560 CACACGTGCA CTACACACAA TCACACGTGC TATGCGTACA CACCACACGT GTGCCTCAGT 1620 GCTACACATG CCTCATACAC ACAACACGTG CACACACCAC ACATGCCTCA CAGTACACCA 1680 CACGTGCACT ACACACAATC ACACATGCTA TGCGTACACA CCACACGTGT GCCTCAGTGC 1740 TACACATGCA TCCTACACGA CACATGCACA TACCACACAT GCATGCCTCA CAGTACACCT 1800 GCACACGTGC ACTACACACA ATCACACATG CTATGCGTAC ACACCACACG TGTGCCTCAG 1860 TGCTACACAT GCCTCATACA CACGCACACA CACCACATAT GCATGCCTCA CAGTACACCT 1920 GCACACGGGT GCTACACACA ATCACACATG CTATGCGTAC ACACACTTGT GCCTCAGTGC 1980 TACACATGCC TCATACACAC GACACGTGCA CACACACACC ACATATGCAT GCCTCAGTAC 2040 ACCTGCACAC GTGCACTACA CACAATCACA CACGCTATAC ATACACACCA CACGTGTGCC 2100 TCAGTGCTAC ACATGCCTCA TACGCACACA CACCCATGCA TGTGTCACAT GCACCGTCAC 2160 ACCATAAGCT 2170
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