| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02634 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:159566760-159568990 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RORA | MA0071.1 | chr1:159567589-159567599 | TGACCTTGAT | - | 6.02 |
|
| | 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 |
| GH01I159596 | chr1 | 159566407 | 159569121 |
|
Enhancer Sequence | ATCTTTGCCT ATCCAACTGG TATCTCAGTG GTCTCTTAAG GCAAATTCCT TTAATTTTAG 60
TGACACACTC ATTTCTACTC GAAACATTTG CCTCATTTTC CATGATGGAC TATTTTCTAA 120
AACACCCACA ATATTTCCTA GATTCCTAGT GGCAGTTCCC TAAGTGTGCC AAAATCCCCC 180
AGCCTGTTAG TGTTACTTGT TATTTAAGCA AAATGATTCA AATCATCATT TGATACATGA 240
TGGAAATCCC AGGCTCACTC ACCAAATTTC TAGCAAATAT TGTGTGTGCT TGTAAGGGGG 300
ATGGGAGGGC AGGAGAAGGC CTTGTATTTC TTCTAGTCAT TACAAGCTAG TGGTTTTTCT 360
TCCTCAGTCT GGAACTTACT CCTTGCACAT ACCTTTTTCT GCACTGTGCC ATCATCCACT 420
TCTCTTTACT TCCTAACTAC CACCAACTGA AAATTATACA TATAAAAGCT TTAAACAAAG 480
TCTCTTGAGG CTCTCAAGGG AGTTTACATT ACAGTATAGT TCAGCAAACA ATTTTAAATC 540
AAATAGTACA CCTCTTTATT CTTAGAATTC CCTCTGCCAA AAAAGAAATC AGCTACTTTT 600
TTTTAAATTC AAGGTCCAAC TTTCTGTTGT GTTGCTGATT CTCTTCTCTC TTTTTCCAAC 660
GACTTCCACT TCTCTCTCTA GTTTACATGT CTCCAAACCT TAAGCCTCTG TTAATACTTT 720
CACAATAAGT CAATTTTGCC AACGGTTTGC CTCCCCTAGA CCATCTAGGC TGGGCCCAGA 780
ACACCTCATC TTCACTCCCA CTGAAGTGTT CCTGAAGGTC AGCTCTCACT GACCTTGATT 840
CTGCTCCCCT ACACTGTCAC CAGAAGCTAT CCACCTATGG TTCTAATTCA GTAAGTCCAA 900
CTCTCTCACC CCCTTTTTTT GTCTCAGCTG TGTGGGCTTT CCCAGGATGG CATGCAATGG 960
GACCCCTGTG CCATGCATAT TGTAAAGGAA AATGCCTCCC TCCATGCGCT ACAAAACAGC 1020
ACATTTATGA TGGCACTTTG AAAAGATATG GGTTGTGGTG TCACATATTG ACAATTCCTT 1080
GGCCAGAGGC TTAACAGTGC CAGCAGTGCC AGAAGATTAA GAAGACAGCA AAAACAGAAA 1140
AGGGAGAAGA TGGTGAAGTA GTTATATAAC ATGAGCGAGA ATGCTCCTGA TTACAAAGCA 1200
GAGAAATTGA CTTTTTTTCT TAGTGTTTTC TATAGTCATT GCTCTATCCC TGTTCTAGAA 1260
TTCAAGTCAT GATAAGAATT TCTTCACGTT GACTTCCTGC ATTGCTTTCA GACATTGCAA 1320
TTAAAGAATG CGAAGAAAGA ACCTCACAGA GGTAACAGAG TTTGTTTTCC TGGGATTCTC 1380
CAGATTCCAC AAACATCACA TCACTCTCTT TGTGGTTTTT CTCATCCTGT ACACATTAAC 1440
TGTGGCTGGC AATGCCATCA TCATGACCAT CATCTGCATT GACCGTCACC TCCACACTCC 1500
CATGTACTTC TTCCTGAGCA TGCTGGCTAG CTCAAAGACA GTGTACACAC TGTTCATCAT 1560
TCCACAGATG CTCTCCAGCT TCGTAACCCA GACCCAGCCA ATCTCCCTAG CAGGTTGTAC 1620
CACCCAAACG TTCTTCTTTG TTACCTTGGC CATCAACAAT TGCTTCTTGC TCACAGTGAT 1680
GGGCTATGAC CACTATATGG CCATCTGCAA TCCCTTGAGA TACAGGGTCA TTACGAGCAA 1740
GAAGGTGTGT GTCCAGCTGG TGTGTGGAGC CTTTAGCATT GGCCTGGCCA TGGCAGCTGT 1800
CCAGGTAACA TCCATATTTA CCTTACCTTT TTGTCACACG GTGGTTGGTC ATTTCTTCTG 1860
TGACATCCTC CCTGTCATGA AACTCTCCTG TATTAATACC ACTATCAATG AGATAATCAA 1920
TTTTGTTGTC AGGTTATTTG TCATCCTGGT CCCCATGGGT CTGGTCTTCA TCTCCTATGT 1980
CCTCATCATC TCCACTGTCC TCAAGATTGC CTCAGCTGAG GGTTGGAAGA AGACCTTTGC 2040
CACCTGTGCC TTCCACCTCA CTGTGGTCAT TGTCCATTAT GGCTGTGCTT CCATTGCCTA 2100
CCTCATGCCC AAGTCAGAAA ACTCTATAGA ACAAGACCTC CTTCTCTCAG TGACCTAAAC 2160
CATCATCACT CCCCTGCTGA ACCCTGTTGT TTACAGCCTA AAGAACAAGG AGGTCAAGGA 2220
TGCCCTATGC 2230
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