| Tag | Content |
|---|
EnhancerAtlas ID | HS133-01949 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:95692270-95694470 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFIC | MA0161.2 | chr1:95693837-95693848 | TACTTGGCACA | + | 6.32 |
|
| | 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 |
| GH01I095227 | chr1 | 95693156 | 95693557 |
|
Enhancer Sequence | TACTGTAAAG GTGACATGCA CTCCTCTTTT CAGCTCCCCG TATGAAGCTG TGGGGCTTCG 60
TTAGGATTAA TCCATTGTTG CATTTGCCCA TTTGTATTTT CTTCACTACT CTCAATGTGA 120
ATCAAGTAAA GACATCAGTA TTAATCTGCC TGCTTAACAC TGATGTGTGT CAACATGTTC 180
AAGGTATGAT AAAATCTGGT AGAAATCAGA GTGGAGGTAA TAAGAAAAGT GAACCATAAC 240
CTATTTACTT ATACACTATA ACCATGCATT AATTCATTCT TGACTCATTC CACAAATATT 300
GAATGCCTTT TATATGCCAG GCCCTGTGCT AAAAGTTGGA GATACAACCA AAGATGACAT 360
AGAAATGCAC CCTCATCTCA TGAAAATCAT AATCTACTGG GATTATAGAC ATATAAGCAA 420
ATACAGTTCC CTACGATAAG TGATGGGGAA GTATAGGATG AGTGGAATTC AGACCTGAAG 480
AATGAATAAG AGTTCACCAG AGGGAGAAGT AAGGAATTAT CTTAGGAAAA AGGGGAAAGA 540
GGTAATGACA AAGTATGTGG TAATATGATC CCAAGAGTAG AAGCTCTGGC TGTGTTTCAT 600
CTGGAAGTAT AATGTTCATT TTGAAACTAA TGAAGCTATC AGTGAAAAAA TGTCTGGCTA 660
ATTAATGTTT TGAACAGCAA TGAGAATCAC GTAAATAGAC AAGGATTTTA CCTAAAACAA 720
CAAATGACAA AGTATTATAG CCTAGCCTTT TATTCTTAGA TAGCTTTTAT ATCACTAAGG 780
CAGAGAGATA GAAACACACA CAGAGAGACG TAGAGAGAGA GAGAGAGAGA GGGGCAGTCA 840
GACAGACAGA AACAAAAGCC AATGTGGTAT TAGCAGGTGG CAATTGTGCT ACAAGGGAGA 900
TTTTTTCTAT TGACTTTTTT TCCCCACTAA AAACAGAAGG AAATAATGTT AAAAAGTGAA 960
AAACAACAGG GAAATGCAGA AACACTCCCA CAAAGGGGTT ATTGTTTTGA TCCAGATTGT 1020
GTTAGAAACA CGAGCAAAAT AGTGCTTCTT TGTTTCATTG CCAGGAAGTA CATCACCGTC 1080
ATTGTGAAAT TCTTGAGATT CAGACCGGCA ATCATCTACT CCCATGATTT CAACAGGCTG 1140
CAGATGACCA CATGTATGAT TTTTTTTTTT TTTTTTTTTT TGAGACGGAG TCTCGCTCTG 1200
TCGCCCCAGG CTGGAGTGCA GTGGCGCGAT CTAGGCACAC TGCAAGCTCC GCCTCTCGGG 1260
TTCACGCCAT TCTCCTGCCT CAGCCTCCCA AGTAGCTGGG ACTACAGGCG CCCACCACCA 1320
CGCCCGGCTA ATGTTTTTGT TTTTTTAGTA GAGACGGGGT TTCACCGTGT TAGCCAGGAT 1380
GGTCTCGATC TCCTGACCTC GTGATCCTCC CGTCTCGGCC TCCCAAAGTG CTGGGATTAC 1440
AGCAATCACT CGATGGCGTG AGCCATCGCG CCCGGCCATG TATGATCTTT TAAGACCTGT 1500
CTCTCCCACT ATACTACAAC TTCTAAGAGA TCCTGTTGCA AACCAGTTTC CCTGGGACCT 1560
GGTGCAATAC TTGGCACATA GTAAGGTGCT CAATAAGTGC TTGTTGAAGA ATAAAGGCAG 1620
AGATCTATCT TTCCAGCCAC ATTTCCTTAA GCTTTCTTCT TCCCCCGCTT ACCCTATGAT 1680
GGGGAACCTC TATCACAATG GCCAAACCAG GCATCCTAGG CCTTCTCCAA TGGTTTTTTA 1740
CTTCTTTGGC AGGACCTTCA TCACTTTATC CCAGGAAATG CTGGTGCCCC TCTGGGATTA 1800
GATTCCAAGT GCCTGGAGGG CAGTGACTAT GTCTCATTCA CTCACAAAAA CACCTGAAAT 1860
TTTACAAAAT GACTAGCATA TAGTAGGTGC TTGTTAAGTC TAAGTTATTT TATCAAGAAT 1920
TTATGAACTT TATGATGAGT TTATTTGTAT CAATAAATAT GTATCGAATT CCTAATCTGC 1980
CAGGCACTGT TTAAGGTATG GAAGATACAG AGGTGAACAA GCATGATAAG GCCCCTGGAA 2040
GCTTACTGGA ACTTTAAATT CTAGTAGAGA CAAACTAGAT CCCTATCTGT CACCATATAC 2100
AAAAATCAAT TCAAAATAGA TTAAAGACTT AAATTTAAGA CCAGAAACTA TGAAACTACT 2160
AGAAGCAAAC ATAGGGGAAA TGGATCAGGA CATTGGTCTA 2200
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