| Tag | Content |
|---|
EnhancerAtlas ID | HS051-15877 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr2:111807230-111808860 |
SNPs | | Number: 3 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr2:111808077-111808088 | ATGACCTTGAA | - | 6.62 | | Esrrg | MA0643.1 | chr2:111808077-111808087 | ATGACCTTGA | - | 6.02 | | LMX1B | MA0703.2 | chr2:111807514-111807525 | GATTTAATTAA | + | 6.02 | | LMX1B | MA0703.2 | chr2:111807517-111807528 | TTAATTAAAAC | - | 6.14 |
|
| | 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 |
| GH02I111050 | chr2 | 111807024 | 111808730 | | GH02I111051 | chr2 | 111808761 | 111808910 |
|
Enhancer Sequence | CCATACGTTC CCAGTCTGCT GCTTCCTACT TTTGGCACCT TAAGGAATGC TACACAAATT 60
AGACTGTTCA TATTCACCAC CAGAATGAGC ATCTTATGTC ATAGATTCCT TGCCCTTGAG 120
TGGAAGACAA GCTTCTTCCC CCCAACCCCC CGCCCCAAGG AACAGTTGTT TTATTTCCTT 180
CCAAGTGACA GGAGCAGAGG CATTTCCAAA TGGTATAACC TGCACTTAGG CTGCCTACCT 240
AGGTGAGCCA AAAGTGTGGA AAACCCTGGC AAGCTGCCCA CCTGGATTTA ATTAAAACTT 300
TGTCTTTGAA GCAGAGAGCA GTAAACAGCA GCAGATCACA AAGGTGCACA CACATACTTT 360
CCCACCACTA AGACTCATGC TTTCACACAG AAACCTTGCA GACTGACCTT GAGGTACAAA 420
TATTTCCATG ATGTCACTTC AGTGCTGTAC CACCAGGAAA CCGCGTGCAC CAGGAATTGC 480
ATTTCTTTAT CTAAAAACCA GCTTCTTTAC CAGGTGTCCT CTGACTTTAG AAATGGGTGG 540
AAAAAAAATA GGGTGTCACT CTGAGGGATT TTCAACTCAT TTGCCTAAGA TGTGATATTT 600
TTGGTCTTTA AAAAAAAAAA AGCTTTCAGT GATGTTAGTT TTATAATAAA GAAGCGCTGC 660
TCATACCAAG TGTTGGGTTT GTCTGGGAAC CCTGATTTTT CAGAGTCCTG GGCGTCTGAT 720
ACACTGACTT AGAATGATAT AGATTCAGGC ACATGGGCGT TTCTTGTTTG CCACGCTTAA 780
TTCTCTGTTT CCTGCTTTAA GTTCTATTCT GCAAGGACCT TTCCTTCCAG GTGCAGGCTG 840
GCTTTCCATG ACCTTGAAGC AGCTCTTGGG CCCTGGATGC TCACCTCTTT TCTCTGCTCA 900
CCGGCCTTTG GTCTTTCTTC CCTCTATCCT GTGTTTTCTC CTACCATTTG CTTCTTGCTT 960
CTCTCTTGTT CTTCTCCTAC TGTCCATCTC TCCCCATTTG CAGGAGGTGA AGCTCCTGGG 1020
CTCCCCTGGA GGTTACATGG GCATCTCAGA GGCATTTTGG GGTACAGAGG GCAGCGACAG 1080
AGCCCAGCCC CAGAGACCAC ACCTCCAGGC CTGCTTCTAG TGGTCCTCAT GGCCTCCCCG 1140
ACTTGGGATG CCGCAGCCCC CTCTGAGTTT CTTCACATCT AGAGTGAGAG GTGAAAAGAG 1200
ATGTAACCAA AGGCCCCTCC TCCTCTCACC ATTTCACCTT CTTGCTGACT TTCATGGTGC 1260
TCTGGCTGGC TTCTCTAGCA CATTCGGTTA GAAACTAACA GATTGGGGTT GGGAGAGGAA 1320
GGCTAAGATG GCCTGAGGTT TCCTGGAATT TGCGTGACCT CCAGTGGCGT TCAGTATTTT 1380
GTGTCTTACC TGTTGGTTTC TGCAGACTGT GTGGCCTCAG CAACAGAGGA TGATTTATGT 1440
GGGCGTTTTC TCAATATTTG CAAATATTTG AACAGGCATC ATCAAAGAAA GAAGTTTCAC 1500
TGAACAAAAA CGTGTGCCGA GTTCATATAT ACTGAAACTA TTTTATGATT TTTTTTAGGA 1560
GATTGAGGTT TTCTAATGTC ACATATCAGA AGGCACCATG TGGGTGTGAC AATGGTATGC 1620
TGGGTTTTTG 1630
|
