| Tag | Content |
|---|
EnhancerAtlas ID | HS187-21678 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr6:119129940-119132270 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr6:119131237-119131252 | TGAACTCCTGACCTC | - | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr6 | 119130200 | 119130800 | | chr6 | 119130766 | 119130831 | | chr6 | 119131131 | 119132128 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH06I118807 | chr6 | 119129095 | 119132311 |
|
Enhancer Sequence | GAAAATCTGG AAAATAATAT ATGTATCTCT TAACCACAGA GATTATTCCT AAACATATTT 60
CAGAGTAATA CTCTTTACAT ACTCCCATCT ACTTTGACTT TCATTTAAGT ATTTTTAACA 120
GCTATGCTGT AGTTATGGTG AGCAATATAT ACACAGGAAA ACGGAAGTTT GATAACTAGT 180
GACACAATAA GTAGCTCCCT CTGTGGCCTG TGGCCTAAGC TGCACTTCTC GTATAGCCAA 240
AAGTGGTTTG CAATCCCTGT AAGGTACCTA GCTGCTATCA GGTCAGGAAT TTACCTAGCT 300
CCTTGGGAAA GATGACCCAA GTGCCTTAAA GCTCTCTTAA TTCAGTAATT ATAATAGAAT 360
CAATAGAAGT GGTATAATTA TAGAACCTTA AACCAAAAGC TCCAGGGAGA TAGAGATGCG 420
GTAGACTGGC CAATCACTGC CTCCCACCCC ACACTCTCTG AGACTGTCTC CACCCAGAGC 480
TCAAGCAGCT GTGTCTATAC CAGGTGGCCA CTCTCCTCAT CCTCTACTCC CTTTCAAGCC 540
AAGATGAACC CACCAAGAAT CTGAACTAAA AAGCTTGAAT CAGAAAGATG TAGGTAGGGC 600
ATCATCTGGC AAGGTCAGAG AAAGTCACAG CTGGAGCCAG GCCCCAAAGT AGTTCAAAAG 660
CCAGAGGGTA GCTGGAGCAG ATAAGCCTTG AGTGAGCACA GAACGTGGGG CTGCTGGGAG 720
GAACAGGAAA CTGGAGCACA CTCATTGAGA GAGGCAACAA CACGGGACCT TGAGGATCCA 780
GGAGAGGCTG AGGGAACAGT TTCAGTCCTG ACTTTCCAGT TCTGGGCCCA TGTGGCCTGG 840
TGAGACTTTG TTGCCTGTCC TTAATGAGAC TCCCTGCTGT ATCCCTACAG CAAACTTGCC 900
TTTATTTCAG CTAGCTTCTG AGGGTTTCCT TTTCTGTAAC TCAGCAATAT GTAATAGATA 960
GGCCTGATCC TCAGCCTTTA TGGACAAGAC CGCTGAAGAC GGCGAAGCCA CACTGTTGGC 1020
TAGTTCTAGA ACCCAATTTG CCTTGTTCTT AGTTTTGTTC TATTACCCAG TCTATGTTGT 1080
TTTTTTTTTT AAATTTGAGA CGGAGTCTCA CTCTGTCATC CAGGCTGGAG AGCGGTGACA 1140
CAATCTCAGC TCAGTGCAAC CTCCACCTAC CGGGTTCAAG CGATTTTCCT GCCTCAGCCT 1200
CCCAAGTAGC TGGGTCTACA GAAGCGTACC ACCTCACCCC ACTAATTATT GTATTTTTAG 1260
TAGAGGCGGG GTTTCACTAT ATTGGCCAGG CTGGTGTTGA ACTCCTGACC TCAAGTAATC 1320
TGCCCACCTC GCACTCTATG TATTATTGAG CACTGAAAAA GTTAGATCTC AAAATAGTAA 1380
GCAATATTCC AGCATTGGTT TTGCTTATCA TGAAAACTGT AAGTTAAACC AAGTTTGTTC 1440
CCACATAAAA ACACACCTGA TACAAATGCT TGCTTTCTGT CGGTTCACCT CTACCAAGGA 1500
ATTGCAATTC CAACTAAACA TAAAGAAGAG TGGCCTAAAA ATAATTTGCA TTCACAAGAT 1560
ATAGAAATTA CTCATTTCTC GGTAAGTCCT GGCCCAGTAT GTATATCCCA TTTCCTCCCT 1620
TAAACTGTAT CTTGCACCGG ACTATTCACA GACACAATTT TTTAAAATTT AGTTTAATAT 1680
CTGTCAAGTT CACTTTTATT ACAAATATTA CCCTTAGATG CATTTTCAAG CCTTTAAGGA 1740
AGAGATGTGG CAGTGGAACA GATACAAGAA CTACTGAGTG TGTCATAAGG GGCGGTTGCC 1800
ACCACTTCCT GTGCATGTCC TCTGAGTGAC AGTGAAGAGG ATGTGTGTGG GTAATGGCTC 1860
CCCGTATACC TGGGGGGCTA TGTCACATGC AAGACAGAAC ACTGACAGGA ACACCCCAAT 1920
TGGAGTGGGT ACTAATGTGA GCCAGGGCGC TTTTATCTTT CTTGAATGTT AATAAGGAAA 1980
GCAAGCTCAG AGGATGGTTT TGAACACTGA GGAAGAAGCA CTGGCTTAGC TTCCTACATT 2040
GTGATGTTAA TAGGTTTGGA AACTGGTTGT TTGGTAAGTT GCATCTGAAA GGTTCACCAG 2100
GTCCCAGGAA GTCTCTAGTG ACCTAGAATT CAAGGTTGGA TAGTTTCTGA ACTCCTAAAT 2160
ATTGTGAACT GGCTAAAGGC AAGCTCTCTG AGTTAACCTA GGATTTTCTC TAGCATTCCA 2220
CCCGTTAAGC AGAAGGTTTA GCACATGGAG AAGGAACAGA AATCAAGTAT GCCTACAGAA 2280
TGTGTAAGTT TGTTAGAATT AAAATTTGTC AACCAAGAAT AAATGTTTAA 2330
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