| Tag | Content |
|---|
EnhancerAtlas ID | HS083-00614 |
Organism | Homo sapiens |
Tissue/cell | HCC1954 |
Coordinate | chr12:121664860-121666050 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr12:121665672-121665687 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28089 | chr12:121664209-121668971 | Fetal_Intestine | | SE_28761 | chr12:121664047-121669000 | Fetal_Intestine_Large |
|
| | 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 |
| GH12I121226 | chr12 | 121664242 | 121668712 |
|
Enhancer Sequence | AGATCGCGGC ATTGCACTCC AGCCTGAGCA ACAGGAGCAA GACTCCATCT CAAAAAAAAA 60
AAAAACCTGA GAGAAGCCCC TTGGTCCCAG CCTTTCTCTG ACAGCAGTGG TGACAGGCTC 120
AGCTCTCCTC CGAGTGCAGC CCTGTCACTG ACCTTGCTCC TGTCTCAGGG CTGGGAAGAC 180
TGTTGATGTT GTCATTCCAA AGATCCCACC TGGATCAGGG GAACATCCCC CACAGAAGGG 240
TTAGCCATAC AGTGCCAGAT TCTCCAGGAG AAATTCACCA AAGAAATGGA GTCCCCTTGG 300
GGACAGATTC AACTTGTATT GTCAGCCAGG AGCTGACGTG GCACTTCTGA GAAGAGGCCG 360
GCGCACCTGC TGGCGGGTGC TTTGTGCACT TTTCAGACAG GTCAGGATCC AGCCTGTAGG 420
CAAATTTACT TTTGCTTTGA CCTGTAAAAC CGGATCTGCC CAGCCTTCAT TCTCTCCCTG 480
GAGAACGCCT GCGGCCCCAA AGCCAGGCCT ACTGATTTCC AGTGAGGCCA CAAATCCCCT 540
CCCTGGTTAG CAATTCAGTT TTCACCGCCT TGGGGGAGAG GGCCTGCCCT TCCTTGAGGG 600
GAAGAACCTG GAAGGCTCGG CTCAGTGTCT TCTCTTGGAA GAGAAGAGTG TGCATGCAGA 660
AGGGTGTAGA AAATGCTAGA CGTGTTTCAT CTTCTTGACA AAATGACATT GTAAGATGTG 720
TGTATATGTT TTTAAAAATA TTACATAGGG GCTGAACATG GTGGCCCACT CCTGTAGTCC 780
AGCACAGGGA GGCGGAGGTA GGAAGATTGC TTGAGGTCAG GAGTTCAAGA CCAGCCTGGG 840
CAATGTAGGA AGACTTCATG TCTACAAAAA AAAAAAAAAA AAATTTCATT AGCCAGGCAT 900
GGTGATGCAT GCCTATAGTT CCAGCTACTT GAGAGGCTGA GGTGGGAGAA CCCCCTGAGC 960
CTGGGAGGTC GAGGCTACAA GAAGCTGTGT TCATGCAACT GTACTCCAGC CTGGGCAACA 1020
GAGCAAGACC CTGTCTCAAA AATATATATA GGCTGGGCGT GATGGCTTAT GCCTGTAATC 1080
CCAGCACTTT GGGAGGCTGA AGCAGGCGGA TCACTTGAGG CCAGGAGTTG GAGACCAGCC 1140
TGACCAACAT GGTGGAACCC TGTCTCTACT AAAAATACAA AAAAAGTTAA 1190
|
