| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02125 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:117017300-117019060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr1:117017850-117017860 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
| SE_27848 | chr1:117013898-117021408 | Fetal_Intestine | | SE_28774 | chr1:117013873-117021547 | Fetal_Intestine_Large | | SE_41250 | chr1:117016870-117021350 | Left_Ventricle | | SE_47846 | chr1:117017467-117019346 | Pancreas | | SE_50584 | chr1:117016337-117019459 | Sigmoid_Colon | | SE_52493 | chr1:117016317-117021272 | Small_Intestine |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I116471 | chr1 | 117014027 | 117021401 |
|
Enhancer Sequence | GATTCAAAAG ACACTGAATC AATGTGTAGT CTAGCTTAGA AGTCCTCGGC CTGAAGATAA 60
AGATGAAGGA AATGAGATAA AGGGAATGAG GCCAAGAAAC AGTGAGGCAG ATGGAGAGAA 120
GGGAAAGAGA GGTACAAAGG TAGTGGAGGA TGCACCCTAA TAACTCCTCA CAGATAAAGC 180
AATACAGCTA CTGCGACCAG CTATCAATGC AGTTCATAAA TGCAGAGATC ATCAGAGCAG 240
GAAAGGACCT CTGTGCTCCC AGCCTCCCCG TGTTACAGCT GAGGAGTAGA GGGCCAAGGC 300
ATCTAGTGGC TTCCCCAAGG TTCTCCAGGC TGCTGTGGAG GCAGAGCCAT GGCCACGGCC 360
CTGGCCTCCT GGCACTCAGG CCTAACAGCT TCCATCAGGC TGTACCACTG AGATTATCAT 420
CATCAGTGAT GATGGTGCCA TTAACAGCCA TGGCCACCAC TATCTGGTTT TTTAGCACCA 480
GCCACCCTGG CAGCCATCTT CATTTTGTGA CTTGAAGAAA GCACTGCCCT GGTCATGTGA 540
GCACAAGAGG AATGGAAAAT TCCAGGTCAG GGAACAACAC ACCCTCCAGG CATCCTTCTC 600
CACCAGCCCT GCCTTCAGAG GCACCAGGCC CTTTTGTCCC ACCACCAGTT AATATTTCAC 660
TTGGGTGAGA CTTTAGAGAA CAAAGAACAC AAAGCTGGCC TTGAGGGGCC AAAGGTAAGC 720
AGCCCATGGT TCCCGATTCG GCTCATAAAT AAGAACAGGG CAAATGTACT TTGGATAAGG 780
ACGCGCTCAG CCTCCCGCAG AACAGCTGGG GAAGCTATTC ATAGGAAAGC GTGCTATTTG 840
CGTCTGCCTG GCATTTGAAT GAGGCTCACC TAACTGTGCC TGCCCTCCCC ACAGATGTGA 900
GTCACGCTCC CCACTCACGA GTGAGGAGTG GCCAGGGGCA AAGGAGAATT GCTTCTCGGC 960
TCAGCTGAGA GAACTGTGGG GGCCAGGAGC GGCACTGCCA AGGATATCTC CCTCCCCCGG 1020
GCAGGGAGGG CCTCCAACTG AGGACACTTA TTCTGTAGTG ATAGAGCCTG ATTCCCCTCC 1080
ATGTGAGAGA GGTGCCTCCT TGGACCCTGC TACTTTGTCC CTTGGCCCTT GGTCAAGCAA 1140
AGGGGACAAT TCTCAGCCCC CAACCCCTTG CCGGTGGCTT TGACTATCTT CTCACATCTC 1200
CAGTACTCGG GGAAAGCCAG TCAGAGCAGC GTGGGAGGCC AGTTCTAGTG TCACGCTGCC 1260
ATCCTCCAAG TTCTACTGGT CCCTGGTCTC TAATTGCAAA GCTTACGTGC TGTGGAGGTG 1320
AAGTGGGGGT GATCCCTCCC CCTTAAGCAG CACTGCCCAC TTCTGAAGGT CATCCACCAA 1380
TGCTCCTGCC TCCTGTAGCA TCCAGTGAAG TTCTGGGCTG GTTCTGAGCC GAGGGTGTGC 1440
CGGAAGCAGG GCTCATTATG GTCCAAAATA ACCTTGGGAG GTCAAGCCCA GGCCTGGGCA 1500
TCCCTCATCC AAGGAGCCCT GATGGGGGGG TCTCTCAGGG CCTAGCCGAA GAGTCAGTTC 1560
CGCTCCATAG CAGCACTGAT GGTTCAGGTC AGTCCCAGGC CCATGAGAAA AACTCCAGTT 1620
CTGCACCAAA ACACAGTGGC CTTTGGAGTC CATCAGACTC CAAGCATTAG GAAGGGCCAA 1680
GCTCTTCTCC CATTGGTAGT TCTCACACAC CTGTGGGTCC AGAGAGGGGC TACCCGCCAT 1740
GATCCTGGGA GCTGTGGTCT 1760
|
