| Tag | Content |
|---|
EnhancerAtlas ID | HS074-08452 |
Organism | Homo sapiens |
Tissue/cell | GM19239 |
Coordinate | chr2:61067650-61068830 |
Target genes | |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr2:61068065-61068085 | TGGGAGGGGGTGTTTTCGGT | - | 6.8 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_60097 | chr2:61021478-61072429 | Ly4 |
|
| | 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 |
| GH02I060837 | chr2 | 61064823 | 61069128 |
|
Enhancer Sequence | TCCGCCTGCC TCGGCCTCCC AAAGTGCTGG GATTACAGGC GTGAGCCACC GTGCCGGGCC 60
CAGAGTTTAC ATTTCTAACA AGATCCCGTG TGATACACAT TTTAAGAACT GCTGGCTTAG 120
AACATCCCTC ATGACTGTGA GTGGTCCCTC ACTGGCTTCA CATGAAAGTT GATGGTTACA 180
AAATTCAAGA TGAAACAACC ATGATAGGCC TTCTAAGCAG GTATTTTGTG AGTTTAAATG 240
AAAAGAGATC CACATGCCTT ATTTAGATAA TGAAGATAAG GATAGCTAAC ATTTATTAAT 300
CTTTTCTCTT TGTAACACAC TAAGGGTATA ACACACATTA TCTCACTTGG CATCTGGCAT 360
GGGCAGCAGT GTTGGTGTTT GATGTTTGGC TGAGGAGCCA GACTTGTGTG CGTGCTGGGA 420
GGGGGTGTTT TCGGTGCACT GTTGTGGTCT GCAGAGGTAC CTGCATGCCA GGCCAAACTG 480
TCCCTCAGGA AACACCTTTA GATCTAGACT AGCAGACGCT AGAGGCCCGA GTTCTGCTTC 540
ACAGAGTCTG CAGGAAATAA ATGAAAGAAG TTGAGGGCAG GTGTTAACAA TCATCTGTTT 600
CAACCGCAAA AGTACCTGAA TATAGAACAG AATTTGTCAA GCCTGGCGCA CAGCAGGAGC 660
ACCTGGATGC CCGGGACCCA TCCACAGAGG GTGTGATTAG ATTGGCCTGG AGAGACACCT 720
GGGCACAGGC ATTTTTAAGA GCTCCCCAGC CAGGGTTGAG AAACACTGGT ACAGGTTTGA 780
TTGCAGCAAG ATGAATCGGG TTGGCTGAGG AAGGGAAGGG GCAGAGACCA AATTGAACAA 840
AACAAAACAT CTATTCCCAG ACTGGATCTC TCTTAAGCAT TTGCCAAATT GGTTTTGTGC 900
TATCCTTTAG AACAGTGGTC TTCAAATTTA GTATGCATCA GAGTCACCTT GAGGTTTCCT 960
TAAAGCAGAT TGCTGGACCT ACCCCCAGAG TTTCTAATTT AGCAGGTCTG GGGTGGGCTC 1020
AAGAATTTGC ATTTCTAACA AGTTCCCAGG TGATGCTGAT ACTGCTGGTC CCAGAAGCCA 1080
GTTTCTTTGC TATTAAGACC TTCATTGCAA CATACAGAAG GATGCCTATA TTTCTTATTT 1140
TCTACTTATT CTCAACTCTT TTTTACTGAA GCAAAAAAAT 1180
|
