| Tag | Content |
|---|
EnhancerAtlas ID | HS051-24151 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr6:139663980-139666170 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr6:139664681-139664694 | AGCAGCTGTTGCT | + | 6.59 | | NKX2-5 | MA0063.2 | chr6:139664525-139664535 | CTCAAGTGGT | - | 6.02 | | STAT3 | MA0144.2 | chr6:139664502-139664513 | CTTCCCAGAAG | - | 6.14 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_09856 | chr6:139663782-139664930 | CD14 |
|
| | 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 |
| GH06I139343 | chr6 | 139664338 | 139664570 |
|
Enhancer Sequence | GATGTATGGT AATCCTTGAT TGAATGCTGG GCATTATAGA TTTTTTCCTT GTTTGGTGCT 60
GGATAGTTTC ATATTCCTAA AAAGACTCTT GGTCTCTTCT TGGATGGTAG ATTGGAGACA 120
TTGTCAGCAT GCTTCTCCTC CTTGGAAAGA CACAATAGTG TGTAGTGTTT CACACTGTGA 180
ATTTTTCTCC AAGAAGCAAC ACAGGAACTA AACAGGAAAA CTGAAAGAAA CCACAGGCCC 240
TTTGAAAGAA GTGGTGGGCT GCAGCCTACA CCATGAGTCA GGTGAAAAAC TAAGTCTGCA 300
GAATCTGAAG GGGGATAAAC TGCCTCCAGG AAATACACTC CCACTGGGGA ACCAGTTAAT 360
CCAGTCCATG GGGGAAGGCC TTAACCCTAC TGAGTGCTGG CATTGATTTA GGGATTGATG 420
TGGCATATAA AAGCAGGGGC AGCAGTGGGA AGAGCCTTGT GTGCATTCCC AGTCTTCAGC 480
ACAGACTAAG GGAAGTGATT TTTGGTCCTA CCTCACAAGG GACTTCCCAG AAGTCTGCCA 540
ACTAACTCAA GTGGTGGTTG CACGTTGAGA GAAGCTCCTA GCTGAAATTC ATGATATAAT 600
TTCAAGTGGG GACAGACTCC CTTGGCCAGA ACTGGGGGCA AGTGGGAAGT GTGCTATAGC 660
CACAAGTACA GGAGCTGGGA CTGGGAGGAG CATGTCCTGA AAGCAGCTGT TGCTGTCTCC 720
ACAGGGAAGG CTTATGGGCT GGGGCAGTTT TGAGTTTTAA GTGCAGATTG CCTGGAACTT 780
AGCTAGCTGA TGCTAGTGTA ACACTGCAAG TATGAGAGAC CTGCCTTTCT TTTTTCTTTT 840
CTTTTTTCTT TTTTTTTTTT TTGAGACGGG GTCTCACTCT TTCTCCCAGG ATGGAGTGCA 900
GTGGAGTGAT CTTGGCTTAC TATAACCTCC GCCTCCTGGG ATCAAGCAAT TCTCCTGCTT 960
TAGCCTCCCA GGTACCTGGG ATTACAGGCA TGTGCCATCA TGCCCGGCTA AGTTTTGTAT 1020
TTTTTGTAGA GATGGGGTTT CACCATGTTG GCCAGGATGG TCTCAATCTC CTGACCTCGT 1080
GATCTGCCTG CCTCGGCCTC CCAAAGTGTT GAGATTACAG GCATGAGCAC CGCGCCTGGC 1140
CTGCGACCTG CCACCTGCCT TTCTAAGCGT GTGGGAGCTG GGTAGGCTTA CTGTTGCCTG 1200
CTATTCCCCA CTCCCTGTGA AACTCTTCTG TGCAACACAG GCAGCTGCAC TGCTTCCTGG 1260
AATATTACCG GAGCAGCCGG AGAACTGGCC CCCAGCTCCT ACTGGGGTTA TTTGCCCTGC 1320
ATGTGGAGAG CCAGAGCATG GACCTGCCTG ACCCAGCCCC CACCTGGCTT TGCTCCACCA 1380
CTTGCCCTGG TAGCTTAACA CAAGGGACAG AAACTTTTGG GAGCTCTATG GACCCACCCA 1440
TTGCCTGAGA TTCTAGAATA CCTCCCCTGA GTTACATAAG GCAAGCACAA ATCCCACCAC 1500
TACTACCACA GCTGACACTC TTTTGCAAGC ACCACCTCCT GGCTGGAGGC CAACTGACAC 1560
AGTCCATTAC AGCATTCTCA GGTAGAATAA CACAGAGCCC AGGAAGGAGA AAACTTGTGT 1620
GTGACCTCAG CTATCACCAT TGCATGCAGC ACCCTGGCTA ACCAGGAGGT TCTGAGTCCG 1680
TCCACGTGAC CAGTCTATAG CTCTACCCCA ACAGTCAGGC AGCCCTAGCA CTTGTGAAGG 1740
GTCTTGGAGA AGCGAACTTC TTTTCCCCCT AGTCCATCAC TGCAGGCACA TCTGGGACTT 1800
CTCCTATGGG AGCTTAGCAT GGGTGCACCT ATAGACAGCC TTTCTAGAAA ACTTCAGGGT 1860
GACTGCATCA CTCCAGGAAG GGCACCCTCC AGGTTCAGGC TTGCATAAGT GGTAGAGTTA 1920
CAATCCCTCT CTACTTAGAA CATCAACATT CCTGCAGATG AAAAGAGGTG CCTGCCTGAT 1980
TTGAATAACT GAAACACTGG GTCAGGAGTG TGATTGGGAG GTGAAGGGCT TTCCTGCTTG 2040
CCTTGCAGTG GAGCTGAGGC AGCTCCCACT CTTCCCCCTG AAAAGACCTC AGTGCATTTC 2100
GCTGAGAGCT ACCCCAGCCA CCTCTGCCAA GGCTGAGACC TCTGCCCACC ATTGGGTATT 2160
GCACTTACCT ACCTGCTTTA GTCATGACCA 2190
|
