| Tag | Content |
|---|
EnhancerAtlas ID | HS002-08197 |
Organism | Homo sapiens |
Tissue/cell | A375 |
Coordinate | chr6:14000810-14003120 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr6:14001709-14001729 | CCCCCAAGCACCTCCTCCCA | + | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr6 | 14001134 | 14001471 | | chr6 | 14001476 | 14002290 |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH06I014000 | chr6 | 14000355 | 14002796 | | GH06I014002 | chr6 | 14003081 | 14003445 |
|
Enhancer Sequence | CCTGTCACTT ACCAAGTTTT CAGGTTGGTG TGAGTTTTCT GGCTTTCTCT TCTGTGTCAT 60
TGTTCTACTC GTTCGGTTCT GTGATGACTC CCCAGTGTTA ATCACAGGAG CTTCATGCAG 120
CTATTAATCT GATATCTTGC AGTAAGAGAC CCCTAACCTG ACTGTCTCCT TTAAAACGAT 180
GTTACCTGGG CTTGGTGGCA TGCTCCTGTA GTCCCAGCTA TTCAGGAGGC TGAGATGGGA 240
GAATCGCTTG AGCCCAGCAG TTCTGAGCAA CATCGCAAGA CCCTGTCTCA AAAAACAAAA 300
CAAAACTACA AAGAGTAAAT TTGTTTCTGC TCATCCCAAT ATTTTGCTTT TGCTATGAAT 360
TTCTAAATCA GTTTGTCAAG TTTTATGAAG TCCATCTTAG AAGTTTGTCT CGTGCTCCAC 420
AGCAAGCACT TACCAGTGCC AGGATGTGAG CCTAGGATAC TGATTCCCAT GGGGAAAAGC 480
AGCAGCATTG CCTCTGAGCT GCTGCTAGCA AGCCAGGAGA GCGTAATTGT CTTGTGTTCT 540
CCCCAAGCTC CTTTAGTGCA TTGGGTCTTA CTTTTGTAAC TTCTACAGCA TGGGGCTGTC 600
CAGAGGAAAC AGCACTTGGT AAACATTTAT TGGGTTTAAC TAAATGTGAA TGTGTGAGAC 660
AAGAAGTCTA GATGCACCCA GCAGAGAGGG TCTCAGAATA TTAACAGCCC CGGGGGGTGG 720
AAACACAGAA TCTGCTTCCT CCAATGAAGT GGCCTGATCT CGTCACTAAA TATTGGAAGG 780
AGGCCACGTT ACAGAGCAGA GACTGAATTT CTCATCCACA TCCGGAGCCA GGCATTCTGG 840
AAATGAGGTC TGTTTGCCAC CTCTCCCCAA AGCATTGATC TCTGATCATG AGTCATTAGC 900
CCCCAAGCAC CTCCTCCCAG CTGGCTCATA AGAATTAATC AGCTTCATCA CTGCAGTCAT 960
TCCCCTCGGG GAAAATGGTC AGCGTATACA CAACAAATCC TTGTTGAATT GGACTGAAGG 1020
GAGTCTAGCT GTTAATCTCT CCTCAAATAT GGCTGGTTGG AGAAAAAGGA ATGTAACGGA 1080
ACATATCAAA GGAGATGTCT CTCCTGGCCG CTTGACAACT CTGGTGGGAT CTTCCCATGA 1140
CCAGCGCTGC TGTATGACTC ACGGCTCCAC TTCTTTCCCT GCCCTTTTGT GGCAGGAAGG 1200
GAAGATGCTG TGCTTCTCAC TCATGAATTG TGCTTCTTAT GACTCAGTCG GCCAGCCTGT 1260
TAGCATTGAT TTGTTCTTGG TGGACACCGT TGGGCAGAAG GCCCTGCTAA CCACAGAAGC 1320
GAGGGTGAAG TGTGCGCTCA CCACCATCAG CAAGGTCAAA ACTCAGAGGC TGTTTATTTC 1380
CATCCAAGTG CCTCATACTT TTGCTGCCCC AGGTGAATGA TGGTGCCTTG ATTATGGGCC 1440
AAGAGGCAGA TGCATGCATG CTTTTCCACA CAGCACCCTT TTATTGAATG CAAAATAGAA 1500
CTTTAAAGAA AAAAAATGGT GAAGTTTAAC GTTAGTCGGT TTTACTAATA ACTGTATTAC 1560
AAAAGCTTGG TACTACATGA AGTGTAATAA TTGGAGCTAT TCAAGTAACG GAAGGTGTTG 1620
CCCCGAGAAC AGTGAGGTCC CATCACTGGA CGTGTTCCAC GGAGACTGCT GAAGGTGAGA 1680
GGTGACAGCG GGCTGGCAGC CCTGGCTCGC TCTCGGCGCC TCCTCGCTTT GGTGCCCACT 1740
CTGGCCGCGC TTGAGGAGCC CTTCAGCCCA CCGCTGCACT GTGGGAGCCC CTTTCCGGGC 1800
TAGCCAAGGC CGGAGCCGGC TCCCTCAGCT TGTGGTGAGA TGTGGAGGGA GAGGCGCGGG 1860
CGGGAACCGG GGCTGCGCGC GGTGCTTGCA GGCCAGCGCA AGTTCTGGAT GGGCGTCGGC 1920
TTGGCTAGGC CCCGCAGTCG GAGCGGCCGG CCAGCCCCGC TGGCCCCAGG CAGTGAGGAG 1980
CTTAGCACCT GGGCCAGCAG TTGCTGTGCT CGATTTCTCG CTGGGCCTTA GCTGCCTCCC 2040
CACGGGGCAG AACTCGGGAG CTGCAACCTG CCATGCCTGA GTCTCCCTCC CGCCCGCCCG 2100
CGGTGGGCTC CTGCGCGGCC CTAGCCTCTC AGACGTGTGC CGTCCCCGCT CCACGGCTCC 2160
CAGTCCCATC GACTGCCCAA GCGGTGAGGA GTGTGGGTGC ACGGCCAGGA CTGGCAGACA 2220
GCTCCACCTG CAGCCCCACT GGGGTAGCAA CTGGGTGAAG CCAGCTGGGC TCCTGAGTCT 2280
GGTGGGGACT TGGAGAATCT TTATGTCTAG 2310
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