| Tag | Content |
|---|
EnhancerAtlas ID | HS060-18649 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr2:8452140-8453920 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFAT5 | MA0606.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | | NFATC1 | MA0624.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 | | NFATC3 | MA0625.1 | chr2:8452983-8452993 | AATGGAAAAT | - | 6.02 |
|
| | Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
| SE_20349 | chr2:8448174-8458311 | CD56 |
|
| | 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 |
| GH02I008312 | chr2 | 8452320 | 8454331 |
|
Enhancer Sequence | CCTTCTGCTC GGTCTCCCTG CCTCAAAAGC AGTGGCTACT CCTCCCATTG TACCCTGCTT 60
CCAACCCATT CTCCACAGGG TAGCTGTGGG AATCTTTCTA AAAGGCAAAT GTGACCCCAC 120
CATTCCCCTG ATTGAACCCT GTGATGGTTC TCTGTGTTTT TTCATTCTCC CCGTGGTGTG 180
GACCCCTGCC CATGCCCTGA GTCCTCCCAG CCCCACCTCC TGCTCTCTAC ATTCACAGGA 240
CCCCAGGACT CCCCTGCCCC AGATGTCTGG AAGTCCCTTC TCTCATTCTT TATGAGAGGC 300
AAGCTCCTGC CTGTCCTTTC AGATCTTCAC TTAGATTTGA CTTCCCCTGG GAGATACTGG 360
TTGGCCCCTG AGATCAGAGG TGGTGCCTCC TCTGTGTGCT GGTGGGGTCC TGGGCTCTAG 420
CCACAGAAGC ACCTGTCAGC TACATGTTGG TGAGATGGTT TTATGGCACC TGGCTCAGCG 480
CGGGCCCTGA TGCAGACAGT CCAGGTGTGA CCCCTGGCTC TGCCATTCAC TGGCTTTGTG 540
TCCTCTGAAA AGCCACGTCA CACCCCTAAG CCTCTTTCTT TCCCTGTAGA ATGAGGACAG 600
CAGCAGCCTC TCCCTCCTCC CTCGGAGGGT TATTTTGAGC CTTGAATGAT TTCATGTGGA 660
TTGAGTGCCT TGAACATGGG TGTATTGTCA GTGTTAAATA CGAGTTAACT AATACCTGTT 720
TTGTCTCCTG TGTTTGCCCC ATGCCTGATC CCCATGCCGG TGGAGGCTGT TTCCATCTTT 780
TGTCTGTGGT CTCCATAAAT GCAGCCAGTG TTGAACACCC AGTAGAGGAT CAGGCACTGC 840
TGAAATGGAA AATTCAGAGA ATGAGTGGCC CATGGAAGGC AGAAGACGTG GGCCCGCCTG 900
CTGAGGGAGA GCAGGTGAGG AGGCCAGAAA CCTATTCCTC ACAGTTTTGG AGGTTGGAAG 960
TCCAAAGTCA AAGTCCAGCA GGTTTGGTTT CTGGTGACGG CCACCCGCTG GCTATGTCTC 1020
CACATGGCCA GAAATGTGCA CCTAAACTGA GAGGCAGGGA GCTCTCTGCT ATCTCTTCTT 1080
GTAAAGACAC AAATCCGATT AAGTCAAGGC CCCACCCTTA TGACTCATTT AACCTTAATT 1140
ACTTCCTTAG AGGCCCCATC TCCAAATACA GCCACACAGG CGGTTAGGGC TTTAGCATAG 1200
GAATTGCAGA GACACAGACA TTCAGTCCAT AGCAACCCTC CTGCCCTAGA CCCCCTGGCT 1260
CTGTATACAG AGAGAACAAC ACTGTCCTCC CCACATTCTC TGGTGTGAAG AGGTGAAAGG 1320
GAAAATCATT TCATCAGCAC TCCACCTAAG CCAGCTGCTC TAGCCACGGC TGCTAATGAC 1380
CAGCTAAGCG TGTCCATTGC TTCTGGAGCC TGAGAATTTG GTTTTTTTGT TTTTTTTTTA 1440
ACAGGGGACC TTATTAGCTG CTAACTGCTG AGATGAGAAA TTGTGGTCAG ACCATTCAGG 1500
TGCTCAGCCT TTCAGCTGAA GTCCCCTCCC AGGGGCCTGC CTCTGCCTCT GCATACTCAG 1560
AATTTTCCAG CCAGTTCAGT TTCTGTCAAG TAATTATTTA CAAATTAGAT TCCCAGGGAA 1620
TACATGATAA GAGAATGTAA GCATGGCACC CTTAAATCAC AACAAACTAT TGCTCAATAA 1680
AAGACAAACC ATTAATCCAA TAGCCAATGC TAGAAAACTC AGGGACCTGC CACAGTACCA 1740
GCCCACAACT GAGGCATTTA TCACCACTTA GTCTTCCTGA 1780
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