| Tag | Content |
|---|
EnhancerAtlas ID | HS133-29680 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr7:129208910-129210670 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr7:129209472-129209484 | AAACAAACAAAC | - | 6.32 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | + | 6.02 | | HES2 | MA0616.2 | chr7:129209328-129209338 | GGCACGTGCC | - | 6.02 | | Nr5a2 | MA0505.1 | chr7:129210127-129210142 | GCTGGCCTTGAACTC | - | 8.25 |
|
| | 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 |
| GH07I129569 | chr7 | 129209123 | 129210534 |
|
Enhancer Sequence | GATCATGAAG TCAGGAGATC AAGACCATCC TGGCTAACAC GGTGAAACCC CGTCTCTACT 60
AAAAATACAA AAACATTAGC CGGGCGTGGT GGTGAGCACC TGTAGTCCCA GCCACTCGGG 120
AGGCTGAGGC AAGAGAATGG CGTGAACCTG GGAGGCGGAG CTTGCGGTGA GACGAGATTG 180
CACCCCTGCA CTCCAGCCTG GGTGACAGAG CAAGACTCCG TCTCAAAAAA AAAAGTCAGC 240
ATCATTAGTC ACATGAAAGG CTCTTTAGGC CAGGCACAGT GGCTCATATC TGTTATCTCA 300
ACACTTTGGG AAGCTGAGGT AGGAGGATCA CTTGAACCCA AGTGTTCAAG ACCAGCCTGG 360
GCAACAGAGT GAGGCCTGTC TCTTAAAAAA AAAAAAAAAA AGTGACATGC CTAATAGTGG 420
CACGTGCCTG TAGTCCTAGA TACTCAGGAG GCTGAGGTGG AAGGATCGCT TGAGCCCACG 480
AAGTTGAAGC TACAGTGAGC CCTGATAGCA CCACTGCACT CCAGCCTGGG TGACAGAGTG 540
AGACCCTGGA TCAAAAAAAG AAAAACAAAC AAACAAAAAA GAAGGTTGTT TAAAGACTAT 600
GGGATTCATA AGTCCCCCCC AGCCATGTCG GCAAAAGCCA AACATAGAGA AAAGGTTATC 660
TTGAAAGGAT TTGTGCACAA GCCTCTTATC TAATGGAATG AATCCCCATG ACATTCACAG 720
GAAACCCACT AGGCTCTTGA GAATTTTATT CCAGCAGAAA TACTGCCAGC TTGGACTGAA 780
AGGGAGAGAG AGAGGATGAA ATGTAAGAAG GCTGTGGATC CCCAAAATTC TACTGGCAAG 840
AAACAGGCTG GTAAAACTAT TCAGCTGCAA ACACCAGCCA TGTTTCATGA AAAAGGAATG 900
ATGACTCAGA GGGCGAAGGT TTGAGCCCAG AGGGTGGGGT GGAGCCTTGA ACCACAGAGG 960
ATCATTACCA GGTCTGGAAA ACTAATGTTT GCCCAGATAG ATTTTTTTTT TTTTTTTTTG 1020
AGACAGTCTC ACTCTGTCAC CCAGGCTGGA ATGCAATGGT GTGATCTCGG TTCACTGCAA 1080
CCTCCACTTC CCAGGCTCAA GGGATCCTCC CACCTCAGCC TCTTGAATAG CTGGGACTGC 1140
AGGCACACAC CACCATGCCC AGCTAATTTT TTTTTTTTGT ATTTTTGGTA GAGACGGGGT 1200
TTCACCATGT TGCCCGGGCT GGCCTTGAAC TCCTGACCTA AGTGATCTGC CCACCTTGGC 1260
CTCCCAAAGT GCTGGAATTA CAGGTGTGAA CACCACTACT CCTGGCCTGC CTGGATAGAT 1320
TTTGAAATTG TATGGGACTG ATGCTTCCTT TTTTCCTTCT GTTTTCTCCC TTTTTTGAAT 1380
GGGAATGTCT ACAATTGCTA TTTTATGGCT GTCTCAGCAT TGTATCTTGG GAACAGATAA 1440
CTTGTTTTCT ATTTTCAAAC ATCCACAGAT GGAGAGAAGT TTTGCCCCAA GAGGGACTGT 1500
ACCAACAACT CACCTATATT CAATTTAAAT GATACAGATG ATGAGATTTG GGACTTTAGA 1560
GCTGATGAGA CTTCACTGAC ATTTTGGACT TGAGTTGTTG CTTCAGTGGG TTGAGACATT 1620
ATGGGTGAAT ATATTTTTGC ACTTAGGACA GATGTGAATC TTTGGGAACC AGAGGGCAAA 1680
CTAAGTTTGT GACAACTTGT TACATCAAAA ATAGGAATCT CACACATGGA CCAACAGATA 1740
TCAATAGATA CTTTTCAACC 1760
|
