| Tag | Content |
|---|
EnhancerAtlas ID | HS133-02957 | Organism | Homo sapiens | Tissue/cell | melanoma | Coordinate | chr1:181482080-181484650 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| JUN(var.2) | MA0489.1 | chr1:181483508-181483522 | TAGAGATGAGTCAT | + | 6.08 | | NR2C2 | MA0504.1 | chr1:181483962-181483977 | TGACCTCTGACCTCC | - | 8.03 | | NR2F1 | MA0017.2 | chr1:181483958-181483971 | CCTGTGACCTCTG | - | 6.19 | | Nr2f6 | MA0677.1 | chr1:181483962-181483976 | TGACCTCTGACCTC | - | 7.42 | | Rxra | MA0512.2 | chr1:181483962-181483976 | TGACCTCTGACCTC | - | 6.88 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | ATTAGAAGAG GCCTGTATGA GAATCTGAAT CATTTAGAAA TGTTATGATT CTATCTAGAA 60
GAAAAGTGTT GTATAAGTCA CTACAGAAGA ACAACAAAAA AAGAAAAGTA TTGTAATGTG 120
TATATAATAA GTTTGTGTAA ATTCTTGGTC CTGCTCAGCT CTATATGTGG CAGAATCCAT 180
TTGAAATTTC TTGTCTAGTC CATTTATTTT TGTTTTAAAT GATTATATGT TCATTAAAGA 240
AATATGGAAA ATACAGAAAA GTCAAAAGAA GAAAAAAAAA TTCACTGATT CAGAAAAATT 300
CCTGATTGTT TTGTGGTATT TCCTTCCAGG CCTTCGATGC TAAGCAAGCT GTCTTTTAAA 360
TGCTTGTAAT TTTGCTGCTT TCTTCCCAAT ATAGTATGAG CATATTACAT GTTATTGCAT 420
ATTTTGGTAA AAATCTGTAA TGACTGATCA GCAGTTTGTT AAGTAGATGT ACACATCTTG 480
CTTCTCATTT TTGCAGTTAC TTGACACTTG GATTCTTTCT GTTTTTTGGC TCTGATAAAT 540
AATTATTAAA GATGCTCCAA CGTACGTCTT TTGGATATCA CATTTTATGA GACATTTTAC 600
AAGGTTGAAG AAGTACTTCT GGAGGAGTAT ACGGCTGTTC TGGTGTGGGG TCTGGGAACT 660
AATGGCTGAG AGGAGGTAGA GAAACTGGTC TGTTTGACTG CATGAGAGAA GACTTCCAGT 720
AGATGTTAAT CTCTCTGCAA ATAAGGGTTG CTACATGGTT GTTGAAGAAG CAGATTCATA 780
GGGACCCATA GGGTTCTTTT GTCAGCGAAG CCAAGAAGGG CCCCTGGGTC CTTGCCTGCA 840
TGTCCAGGGG GTGTTCAAGA GTCAGTGCAG GTGCTGAGCT TGGCTGAGTC AGTTGTCCTC 900
TCTGTGCTCT CTTTCCCATC CCTCACATCT TCCCTTCTTA GTGGCTCTTC AGATGTCCCT 960
GGCTTTGTGA ATTGCCTTCA CAGGCCCCTG ATTTCCATAT GAACTCACAG GACTTTGCTC 1020
CTGCTCCTCC TCCAGACCTG CTGCTTAGCC CTCTTCTCAG CATGGACCGT TCCCTTTCTC 1080
CTCAATTCAT GGGTGAATGT GCTCCAGGCA AAGAGCTTGG TCCTCTTGAG ATCCCTGCTG 1140
AGGGGCTGAG GGTTGCGGTT CTATCCCACA GGAATGCATG ATCATATTTA GTCTTACAGT 1200
CACATGATGC TCTCATCTAC CACATTGTGT GGCTCTAAGA TGCACGTTTT TCATGCTGGA 1260
ACATTGCTGA AATCAGCCTG TGTCTTACAA TAATGGCATG ATATAGTTTA ATTGACAGCA 1320
TGTTTTTCTT TCTTAGTGCT ACATAAAATT ACGGGGCATC TTACAATTGT TGGGGTTGTA 1380
GATTCAATGA CATGTGATAC CAACCAGGGA GGCAGGCAAA GTGGACTTTA GAGATGAGTC 1440
ATCTGGTACT CAAAGAGGGT AAGTTATTCA CCCAAGATCA CACCTGCCTC TTAATGGCAG 1500
ATGCAGGAGT CAGAATTGTG CCTTTTGATC CAGGGCTGGT GTTTTGACCC CTGCCCTGTG 1560
CAGCCTCCTT ACCAGGCCAC CTGGTGTCCC CCTTTGTCTT CCTGACACCT GCACCCACAG 1620
CAGTCCCTGC TGACAGCTCT TCCTTCCCAC CTCATCTCCA GGTGTCACCT CCCATTTTCC 1680
CCTCTGCACA GGAGGAATGA CAGGTGCTGG AGCATGACAC AGTGCCTCAG GGCTGAGGCT 1740
GCACAACTTC TCAGCTCTCG GTGCTGACAG GAGGGAAGTG GGTGCTGAGG TGTCAGTCAG 1800
CTGGCTCAGT GTAAGACCTG CTCTTATTGA TCTTTGCTGA GAGATGACTA GTTGAGGGGC 1860
CTGGGCTACC ACATTCTGCC TGTGACCTCT GACCTCCTAA ACTTTAGTGT TCTTTGGCCT 1920
ATAAGTTGAG GGTGTGCATG GTTTAGAAAG CGCATTTATG TACATTGCTT CATCTTGTCC 1980
TCATAATGCC ATAGAAAAGA CCTTGCTAGC CTCATTTTAC AGATGAAGAA ACCGAGGATC 2040
AGAGAGGGCA CATGAATTGC TAGCAGGCAC TAGATCCAGG ACTTGAGACC ACATCTCCTG 2100
GCTCCAAGTT CCTTCTTTCA CTGACTTTTC CCCATACTGG CAGTTACTTC ACAACCCCAA 2160
GGGCCCCATG GTTCTAAGGC TCTGTGGTTG CAGGTTCCTT TAGTCCCCGT GAGGCAGTGT 2220
GGGATGAGCT CAGGGAGGTA TGATCAGGCA AATGTTCACT CTCAAAGGTG GGGCTTCACA 2280
TGTGAGTTGA AGGGGACAGG GGCCCAATGT GTCCATCCTG AGACTTCTCT CTGTGGGCTT 2340
GGGATGAGAC TCCCTGCTCT GTGGTAAAGA AGGCATGTCA CTTTAACTGT CAGCATAGCA 2400
TGGTTTGATG TGTAGAGAGT GGATCAGAGT TCCAGCTGAT TTCTTCCTTA AATGGCTTGT 2460
TTGTTCACTC ATTCACTCAC CAATTCATTA ATTCAGTGAA ACTAGTATTG TGTTGGTGAA 2520
GGCAGAAGGC AATGCTGGGA CCGAGAAATG TGGACGTTAT TATATTTTCC 2570
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