| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29279 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:101241180-101243350 |
Target genes | | Number: 19 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr7:101242482-101242497 | TGCCCTCTGCCCTCT | - | 6.62 |
|
| | 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 |
| GH07I101597 | chr7 | 101241215 | 101243058 |
|
Enhancer Sequence | AGAGCTCCAG GCCACACTGT TCCCACTGTA GGGCCTACAC TAGCTGTCTC CATCTTTGTC 60
CCCTGCCCAT CTTCCTCCAC TAGGGCTCAG CTTGACAACC CTTCCTCATG CAGCCTACCA 120
CCTCTAAGCC TGCATTCCCT CCCTTCTCTA TGCTCTGAAG TTCTGTATAC AGGACTTGCC 180
TCTAAGATCC CACTGGCCAG GTCGTAACGT TGAGACCCAA CCACTCATTC TGCTCCCTGG 240
GCTGGGTGCA CCTCGTGGGT AGTCATTGGC CTTATTTATC TCTGGGCCCC CCGGGAAGGC 300
ATGAGAGCCA AGCTGCTGAA TACAGGGGCC CTGCAGCTTG TACTGAGCAT TTGAGTACCA 360
GACACTTCTA GGATTTCACG ATGGAAGACC CTATGATACG GCATCTCCTT CCCATGCCCC 420
ACTATCAGGG ACAAGGGGTG CAGAGACAAC GGGGCCTCCC AGCTGGAGGG ACTGTTCAGG 480
GCCAGCTCTG AGCTGCCTCC CACCCTCGCC TAGCCTCTGG CAGGGCCTCT GGCCAGGCAG 540
GAACGGCCAA CAGAGTCACC TCCTGCTGAC AAGCCTGGCG CTGACAGCCA GGATCTGGGA 600
GAACAAGAAG TCCATTCAAG GCGCAGGGCC GGGCGGGCCC ACTTTCAGGT GTATGATCTC 660
ACCTCTCGGA AACTGGCAAG CCGCCGGAGG GCCTCGTCAA GGCTTTGATG ACCCTGTGCT 720
GAGGACGCAA ATCCTAGGCC TGGCCGACAC CCTGCTCCAA GGACCAATGA CTGAGGCCAG 780
AGAGGGTCCC AGATGGAGCC TGGGTAGGGG TGAAACTGCA CAGGCGGACG GGCAGAGCGT 840
CCACCCTGGA GAAGAGACCC AGGCCCAACC AGGCCCCAGA GCCTGCACGA GCACCTGGAG 900
TGGCAGGGAC AGCCCAGCCC CCTCCTGCCC CACTTCCTGG GAAGCAGCAG CTTGTGTGTT 960
CTGGTCGGTC GGCTTTGGCA AAGCTGACTG GTGACGTCAG GCAGGCACCC CCTCTCATCC 1020
AGATCCTGGG CCCCCCACAC ACTGGGCCCA GCTGGGGGAT GGAGCTAAAG GAACTTTGCT 1080
CCCAGCTCAT CTTGTTTCTG GGCTTTGTTG CCCAGTGGCC ACTGGCACCC TGGTGGAAGG 1140
GACCAGCCAG GGGGAGTAGT AGGCCCCATC TCAGCTGGAA TCTCCCAGGG TAACTGGGCC 1200
TGCAGCTTGC TGGAGTCCGT ACTTTTCTGT GAGCTCACAG GGCAGATCCC AGAAGCCAAA 1260
ACTGACCCAG AGGGAATGGA ACTCAGATGG TCAAGAAACC ACTGCCCTCT GCCCTCTTGG 1320
CATGTGACCT TAGTTCCACC CATAGAGACC AGATGGCAGT CTCTGGCTTT TCCAAGGACC 1380
CGCGGGGCAG GAATGCAAGA CAGAGCACAC ACTGGCCTCT CACTGTGACC AGCAGTGGCC 1440
TCTGTCGTCA CCTCTGTGGA CGGCAACACG GGCCTTCCAT CCATTCCCCA AAAGGAAGGC 1500
AAAGCCACAG CACCCATGCA GGGGCCGAAG CCTCACGGGA GGTTCCCCAT GCCTTCGAAA 1560
TGACTACTCT GCTCTGGCCG GAGGACCCGG GTCCTGCCAC CTGACCTGAG AGCCTCTCTC 1620
AGCTCAGGTC CTGCCTCCTG ATCACTCGCT GAGCTTGGCC TCCCAACAAC TGTGATGACA 1680
ACAGGCTGTC TACTGCCTCT CGGAGCTCCT CCTGCCCTGG CGGGCCTGGC TCATTGGTGC 1740
CCTGGATGGC TCCCCATCTC CCAGCAACCG GGACTTCTCC CTCCTCCAGG CCCCCGGGAC 1800
TCTGCCTAGC CCATGCCCTG GGATGTTTAT GGATGTGTCC ACTGCCCAGC TTCTCAAGAA 1860
CAGAGGCTGG GTGTGAGCCC ACACCGATTC CTAGTGCTTA GCATAAGCCT GGTCCAAGGA 1920
GGCACCCACT GGTGGTTTGC AAAGTGAAGT CTCTGGTAAT TGAAAGGGCA GTGTGACCAC 1980
ATCCTTGGAG TGGAAAGATG ACAGGCTTCG AGAGCAGACA GCCGTGGGCA GTTGTGGCCC 2040
TTGGACAAGT ATCTTAGCTT ATCTGAGCCT CAGTTTCCTC ATCTGCAGAA TGGGAATATT 2100
AGCACCTATT CCCCTACAAA ATAGCACAGC AACACAAGGC TAAAGAGAGG TGTTTGTTGT 2160
TTTTGTTTTT 2170
|
