| Tag | Content |
|---|
EnhancerAtlas ID | HS023-19155 |
Organism | Homo sapiens |
Tissue/cell | CD8+ |
Coordinate | chr4:6989290-6991640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESRRB | MA0141.3 | chr4:6990150-6990161 | TCAAGGTCATT | + | 6.32 | | Esrra | MA0592.2 | chr4:6990149-6990160 | CTCAAGGTCAT | + | 6.02 | | Esrrg | MA0643.1 | chr4:6990150-6990160 | TCAAGGTCAT | + | 6.02 | | IRF1 | MA0050.2 | chr4:6990602-6990623 | TCTTTCTTTCTTTTTTTTTTT | + | 6.25 | | IRF8 | MA0652.1 | chr4:6989954-6989968 | ACTTTCAGTTTCGT | - | 6.79 | | IRF9 | MA0653.1 | chr4:6989954-6989969 | ACTTTCAGTTTCGTG | - | 6.25 | | Nr5a2 | MA0505.1 | chr4:6990146-6990161 | GAGCTCAAGGTCATT | + | 6.51 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_27343 | chr4:6987640-6990525 | Esophagus | | SE_27343 | chr4:6990735-6991836 | Esophagus | | SE_27664 | chr4:6986645-6990188 | Fetal_Intestine | | SE_28549 | chr4:6986220-6990418 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GGTACTCTTT GTGTCTGTGT TTCCACGTAT TTTCTTCTGG TTCACGTTTA CTAGGACGAC 60
GAGAGACAGC GTGAGCGAGC ACGTCCTTTG AGTCCTCCTT ACCCTGTTTT CAGAGCCGGG 120
CCAGGCCCAG CAGCCCCCTT AGAGGTCAGA AGGGCCTCGC CTGCGATCCG ATGAGCCTTT 180
GTATGGAGAT GAGACTGCGC TCCGAGCTCT AGAGCCCAAT GAGGTGGTCA GGTTGCAACA 240
GCAACCGGGC GTGTTAAAAC CTAGTTCCTT TGAATATGTT TCATTCACCA GCCCGCATAT 300
TAACTTTTGA TGCTCTGGGA GGAATATGAC TATTAGAAAA GGACTCCTGA GAGTGCTTCC 360
CAGAATGCCA ACATTCCCAG TAACTTAGAG AACGCTTTCC AGGAGGGGAC TGCAGCTTGT 420
TAAAGAACCC AGGCCAGAGG AACCACTCAG ATGTTCTCAG TGGCTTTACT TACTGTGAGG 480
TCAGGCTTCA GGGGTTAGCC GGGGCTGCCT TTTGGAAGGT GGGACCTTTC TAAGACCTGT 540
GCAGGCCATT CTTCCCCCTC AAAATGGCAA AACAGCCCCT CCCAGATGCT AAACTGGGCT 600
CCCCCCTCCA AGACAATTGC TTTTACAAAT GGCCAAGTGT GAGACCAGCC GCGGTGTTGC 660
GGACACTTTC AGTTTCGTGC CCTTTTCCAC AAGCAACCCT CTTAGAGTGG AATGTTGTGA 720
AGAGTAATTT CATAGTATAT AGTGACAGTC ATACTCCTAT CATTTCTGGG CACCTGCTTT 780
GGCTCTGCAG CTTATGCTGG TTCTCATTTA ATCTTCAAGT GTAACAGATG AGGAAACAGG 840
CTTGTGGATG GAGGAGGAGC TCAAGGTCAT TCTGCTGGTG GTGCTGGCTC AGACCAGGCC 900
TGCCGCTGTC CCCCAGCGCT TCCCTGGGTC CTCAGCCTGT GCAGATGTGG TGGCCGTGCT 960
GTCACAGCAT TAGTTCAAGT CAGTCTTTTG ATAGGTACCA CTCGGATGGC CAGCCTGCCT 1020
TGGCAGCTTT ATTCCAGGCG CGCTCCCAAA TCCTCAGGTT ATTTTCACTG GTGAATCTTG 1080
ATACTGCAGA CAGCGGGGTC GGAGATTTAA GCACAGGATT TGACTGATGA CCCTTTCCTC 1140
TTCTAGGTAA AATAGATTTC CAGGGAGCCA GAGGCTCCTT CCTGGAAGTC AGGGGGCTTC 1200
CAGTAGCAGG TTATTGACAT CATTGGCTGT TTTGTAGTGT TCCTCCAGTT CATAAGTAGC 1260
ATTGATGACC TTTCTTGTCT TTCTACCAGG AGTACTTTCT TTTTTCTTTC TTTCTTTCTT 1320
TCTTTTTTTT TTTTTTTTTT TTTTTGAGAC AGGGTCTTGT CCTGTTGCCC TGGTGCGGTT 1380
ATGGCTTACT GCAACCTTGA ACTCCTGGGC TCAAGTGATC CTTGTCTCAG CCTCTTGAGT 1440
AGTTGGGACC ACAGGCACAG CACCTCTGTG CCAGGCTTAG GAATACTTCT TCATTGTTTG 1500
AGAATCATGA TCCTTTCTTT TCGCTCTTAA AACAAATGTG CATTGAAGCA GGCTTTTCCC 1560
CCGCTTTTTA AACCAACAAA CGTTAAACCT AATTCAGGAG CCTCGTGCCC TTCTTGTCTT 1620
TAGCACTGTG CAGATCACAC GTGGAATGTA GACCCTGCCC CTGGATGCGT CTGAGGGGCT 1680
CCCCATACCT CATAGTCTCT CCTCTGGCTC TCCTCTCTCT CCTGGGGCTT GTCCCAGCAC 1740
CTCTGGGTAA CGTGTTGAGA CCTTCAAATC TAGAGCAAAA CAACTTTGAC TCTGCACCAT 1800
TCCCGGTTCA AATCCTGGTG CTAGCCTGCT TGTGGGTGTC TCTTGGCCAC TGCTTCTGCT 1860
GTCAGAGTGC CTCTTCCTCT TGGCCTCTAG CCCACGTCTT ACCTGTCTGT CCACTCAGCT 1920
GGCCCCTTTG TGAAAGCTTC CCATGTCCCC CTGGCCTCAG GCATCCTGCC CTTCCTCCCA 1980
CAGTGTGTGG CTCGCCCCTC CTGGCACATC TCACGGTCTC ACCTGTGTGG GAGCCTCTGC 2040
CTGCATCGTA TTGCCCCTGT CGAGTGAGCC CTGCTGGGTT GGAGATTGAG GATCTCCTAA 2100
ACTGCCAGGC CCGCGTGGTC CCTTCACAAA TTAGTTTCCT CTTTTCCACA TGGCCCCTTC 2160
CCTCTTGCCC TGCATGCTGA GTCTCATGCA GAGCCCTCTG CATGAGACTG GGGCTCTGCT 2220
CAGGCACCCT GCCTCCCTGC CTTTTTTCTT CAACCTTAGC TGGGTCATCA GACCACACCC 2280
CACAAGTTGG CTGCTAGTGA GGTGCTGCTG CCATGTTGGT ATGGTCTCGT CTTTCCCAGC 2340
GTGATTCCTT 2350
|
