| Tag | Content |
|---|
EnhancerAtlas ID | HS133-03798 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:230842700-230845180 |
Target genes | |
SNPs | | Number: 2 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr1:230843972-230843993 | TATTCTTCCTCCTCTTCCTCC | - | 6.98 |
|
| | 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 |
| GH01I230707 | chr1 | 230843691 | 230845900 |
|
Enhancer Sequence | CTCCCCCATC ACAGTCATAG AATACAGAGT GGGCCACGCA GGCCCCGGAA ACGAGGGCTC 60
CATTCCTCAG CAGCCCTTGC TACTGGGGAG ACTCACACAA CCTCGTTGTG ATGAATGGAT 120
TTGCACACTG GGCCTTGGGG GCAGGGGTGA GCCCTCTGTT TCCCCTCCTG CTCACAGGGC 180
CGTGCAGATG ACAGAGAACT CGGGAGAGCC CGTTGTGGGA GAAGGACACA AATTTGTGTG 240
TGACGCAGTT ACCTGGGGTC TTTCCATGAC AGCAGCCCAC CCTCTGCCTC GACCTTACAC 300
TAGCACATCC CTGCCCTCGG CTGTCCTCCC ACTCATCCTG AAAGGCCTAT TCTGCGGTTG 360
TTCTTAGGAG AATAGGGTGA AGTTGTGTAT AAGTTTGTCA CAGAACAGTC CCCTGGGCAC 420
GTGGCACTTG GGAGTCTGAG TAGAGATGGT TCAGAAACAG TGAGGTCTCC CTTTGTACTG 480
AATTGGAGGT CCCAGCATGA AAGTAGGGCA GCTGGGAGGA CAGAACTGGC AGGCAGGAGC 540
TGGGCATGGC TGTGCCTCCC CTGGGTCCGG GTCTCGTAAG AAGGCAGTGG CAGACCTGGC 600
ATATTTCTCG TCCTCAGTCC TCGGAGCACT CAGTCTCGGA AGGGCATGTG AGCGGGAAAC 660
TGCAGGGTTC CCCTTGCACG TTCCCTGCAG GGACCTCGGT GCTGCCCACC TGGGCTGGCA 720
AGGCTTTTAG TTTAGAGGGG GGAAAGGGAC AATTCTTTTC TTCCAACAAA CTAAACTAAA 780
AAAGGGAAGC TGCCTCCCAA AAGACGCTGG GATTTGACAT GAGAGTGGCT GCCGTCTTCC 840
CTCTGCTCGT CTGACATGCA CAGCTCACCA TTCTCATCCG GAGGCTAGGT AAATCTGTCG 900
AGGTCAAGTC AGGACCTGGT GTCATGGAAA CCACCAGGGC CAGCGCCCCA TGCTCAGGAG 960
CACAGCAAGC ACTGGGCAGA CGGTACCCTG GAGCCCATCA GGCCCCAGAT CCTCAGGTCC 1020
TCTCTAGTGG GACACATCTA GCTGCCTGCT GAGGTCATGT AAATAGAACA TCATTGCTAA 1080
AGGGAAACCT AGAGGTCCCG AGACAGCCCC CGATCTCCTC ACTGGACAGA CCATGTGGGC 1140
AGGAAGTGGC TGCCTCCTTT GACGGAAACT GAGGCCAGCA AAGTTAGGAA GTGGGGCAGG 1200
GTCAGGGCAG CATGCGGTGG AGGCCGGCGA GGATCCTGGG CTTCCTTTGA GTCCCGATGT 1260
GGTTGGCTTT TTTATTCTTC CTCCTCTTCC TCCTGGCCTG GCTCTGCGGT CTGGGTCAGG 1320
TGGATGTGCT CTCTTTCGAA GGGAGACCCA TTTCAGATGC CACTGGCTTT CTTGCCTTTG 1380
CCTTCTGCAG GACCCTCCTT CTCAGTGAGC GCTCCTCCCA GCACTTCTCC TAGGGACAGC 1440
AGGCTAAGTC CATGTGTCCC TGCTCTGCCC TGCACAGTGT GCTGCCACCC TCAACCGGGC 1500
AACCCTCGGG CTGGCCTCTG CCCCTGTGAC CAGTCAGTGC CAGGGCTGAG CAATCCCCCC 1560
ATCTATCACC TCTCCCTGAA CCCGAAGGGA AAGACCTCAA GGAGGTTGTT GTGGTAAGAA 1620
AAATCACTAT GCGCCACTGA ACCTCTTTCT CCACAGTCTT GTCTTTCACC TCCCGCCTGG 1680
CTCTCTGTCC CTCACGAGGT TAACATCTTG ACAGAGCCTC CTCAGTGTCT CTTAGACACA 1740
CCCCTCAGCC CCACCCCACC CATGGATTTG CCGAGCTGCT CCCTGAGCAC GTGTTCCCGT 1800
GACTGTGTGC CTGGACTCTT GCGTAACCTT CAAACAATCC TCCCTGCCTC CAGTCTGCAC 1860
ACGGCAGGCT TCCGGGATGA CCTCTGAACA GAACGCGTCC CCATTCCCAC ACCTACCAAG 1920
CATGGCGTTC AAAGTGTCTC CAGCTCTGCC CTCCCCAGGC CCATTTTCTG GTTCAACACT 1980
CATGCCAAGC CAACCGCCCC ATCCTCGTTC CTTGCCCCAA ACTCTGCAGG CTGGGCTCAT 2040
CATGCTTGCT CCTAGCTTCA CCAGCCCTGT TGCCCTCACT GCCAGGCAAG GCCTGCTCTC 2100
CGCTCCCCAG TGACCTCTGT CCTCTGAGAG CCCCGAGGCT TCCCTGAGTT ACCTTGTGGA 2160
GCACGTTTCC CTGCAGCTCC AAATCCTAGG CATTTGCCCA TTGACCTTTA AAAGCCTGGA 2220
GGCAGGGCCT ATACAGCCCT CCTCTGGCCT CCTCTGAGAT GCCAGGCTTA AAGTCTTACA 2280
AGTAGCAAAT CCTCAACAAG TATTTGTTAA ATGAATGCTT TAAGCAATCT GTGGCTGGGT 2340
GCAGTGGCTC ACACCTTTAA TCCCAACACT TTGGAAGGCA GAGGTGGGAG GATCGCTTGA 2400
GGCCAGGAGT TCAAGGCTAC AGTGAGCAAT GATGGCACCA CTACACTGCA GCCTGGGTGA 2460
CAGAACAAGA CCCTGTCTCA 2480
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