| Tag | Content |
|---|
EnhancerAtlas ID | HS133-00861 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr1:27396690-27398100 |
Target genes | | Number: 28 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr1:27396717-27396732 | GGAGGGCAGGGGTCA | + | 6.26 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I027071 | chr1 | 27396941 | 27397090 | | GH01I027070 | chr1 | 27397346 | 27397995 |
|
Enhancer Sequence | AGGGGACTTG GGGGAGGCAG TGAGGGTGGA GGGCAGGGGT CAAGCACCCA GGGCCTCAGG 60
TCATCTGTGT CCATCCCCTG AGGCAGGCTC TGGGCAGCCC TCCCTGAGGA GGTAGCCCTG 120
TCCCCAGGGC CCTGGATGGT GAGGATGACC CAGCCTTCGT AACCCTGCCC TCACACACAG 180
CGCTCACTCC AAAGCTTGCT GGAATCATCT GAGGCTACCA GTGTCTACAG CACATCGAGC 240
TACCCTTATG GAGCCTGGGA CCAGCCCCAG GAAGCCAATC TCAGCTCAGG AGCCAGGATT 300
TTAGTGCAAA GCTGCGCCCC CTTCTGTAAA CCATGGTTCT CCTGAGAAAC AGCTCATGCC 360
TTTGGTAAGC TCCTGGGCCC TGGGGAGATG GAACACCTGA CTTGCGGCAC CTGGGGACCA 420
TGTGACCAGA GCTGAGCACT GTCTGACCTT GCCACAAAGT CAGGTGTGCC CAACGGTTTC 480
TGTCATCAAG GGGAGAAAGT ACACGTGGGT GAGGGCTGAG CGCAGGCATG TCCTGAAGCC 540
CAGCTGAGCC TCTCAGCAGG CAGCTCCTTC CCCAGAGTCC CTTCTCCAGC TTCCCAAAGC 600
CCCTGCGTCC GCCCATACCT TGGGCACAGG TCCCTAAGAC CAACTGAACA CTCGAGCATG 660
AGCCAGGCAG ACAGCCTGGG TGGATGCCAG CAGAAAGATT GGTGAAGACT GGATCTCCTG 720
GGCAGAAGCG GTGACAGGCA CATGGCGTCC AGTGTGAGGC TGGAGGCATC AGGGAGCACA 780
GGGATGCAAG CCCCTCTACG TTCTCCCTTG TCATGGCTGG GTGTGAGAAT GACCTTAGGC 840
AATGGGGTGG GGCATGAATA TTTTGAGCTT GTGCCAGCTG TGTGGTGGAG CGTGGGCCTG 900
TACGGAGGCA CTGCACTCCC ATCTCCCTCG GCTCCCAACT CCCTCCGTGG GAAGCTGAGT 960
TCAGGCACTG CCCCTCCTGT ATGGACAGGG AGCCACTGGT CCCAGCTTGC TGGTTGCCAG 1020
GCAACCCAGG ATGAGCCTTC GAGGTCATTC CTCAGACAAC TCTGAGCTCT CTCCACAGCC 1080
TGGGAACAGA TGGTTCCGCA GCAGCCAGCC CCAGCCTGAA ATGAGTTGCG GAGGCACTGC 1140
TGCCTGTCTC CACCAGCAAG AGGGAGGAGA GGCCCTTCCC GTGCCTGCAG CAGTCCAGGG 1200
TAGATGCAAG CAGAAAGACT GGTGAAGACT GGAGCTCCTG GGCAGAAGCA CTGACAGGCA 1260
CGTGGGGTCC TGTATGAAGA GCTGCACTTT GTGTGAAAGG AAAGGTGGCC CAAGGTCTGG 1320
CTCTACTTCA GCCGGGGCAG TGGCTGGTGG TCTTGCCGGG TGGGCCAGTC TTGGGAGGGG 1380
GTGATGGGGA AGTTGGTGAA ACAGAGGCAC 1410
|
