| Tag | Content |
|---|
EnhancerAtlas ID | HS147-12212 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr12:121664710-121665980 |
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: 2 | Chromosome | Start | End |
| chr12 | 121664724 | 121665671 | | chr12 | 121664970 | 121665566 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH12I121226 | chr12 | 121664242 | 121668712 |
|
Enhancer Sequence | TTTGAGACCA GCCTGACCAA CATGGTGAAA CCCCATCTCT ACTAAAAATA TGAAAAAATT 60
AGCCAGGCGT GGTGGTGCAC GCCTGTAACC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA 120
TCACTTGAAC CCAGAGGTTG CAGTGAGCCG AGATCGCGGC ATTGCACTCC AGCCTGAGCA 180
ACAGGAGCAA GACTCCATCT CAAAAAAAAA AAAAACCTGA GAGAAGCCCC TTGGTCCCAG 240
CCTTTCTCTG ACAGCAGTGG TGACAGGCTC AGCTCTCCTC CGAGTGCAGC CCTGTCACTG 300
ACCTTGCTCC TGTCTCAGGG CTGGGAAGAC TGTTGATGTT GTCATTCCAA AGATCCCACC 360
TGGATCAGGG GAACATCCCC CACAGAAGGG TTAGCCATAC AGTGCCAGAT TCTCCAGGAG 420
AAATTCACCA AAGAAATGGA GTCCCCTTGG GGACAGATTC AACTTGTATT GTCAGCCAGG 480
AGCTGACGTG GCACTTCTGA GAAGAGGCCG GCGCACCTGC TGGCGGGTGC TTTGTGCACT 540
TTTCAGACAG GTCAGGATCC AGCCTGTAGG CAAATTTACT TTTGCTTTGA CCTGTAAAAC 600
CGGATCTGCC CAGCCTTCAT TCTCTCCCTG GAGAACGCCT GCGGCCCCAA AGCCAGGCCT 660
ACTGATTTCC AGTGAGGCCA CAAATCCCCT CCCTGGTTAG CAATTCAGTT TTCACCGCCT 720
TGGGGGAGAG GGCCTGCCCT TCCTTGAGGG GAAGAACCTG GAAGGCTCGG CTCAGTGTCT 780
TCTCTTGGAA GAGAAGAGTG TGCATGCAGA AGGGTGTAGA AAATGCTAGA CGTGTTTCAT 840
CTTCTTGACA AAATGACATT GTAAGATGTG TGTATATGTT TTTAAAAATA TTACATAGGG 900
GCTGAACATG GTGGCCCACT CCTGTAGTCC AGCACAGGGA GGCGGAGGTA GGAAGATTGC 960
TTGAGGTCAG GAGTTCAAGA CCAGCCTGGG CAATGTAGGA AGACTTCATG TCTACAAAAA 1020
AAAAAAAAAA AAATTTCATT AGCCAGGCAT GGTGATGCAT GCCTATAGTT CCAGCTACTT 1080
GAGAGGCTGA GGTGGGAGAA CCCCCTGAGC CTGGGAGGTC GAGGCTACAA GAAGCTGTGT 1140
TCATGCAACT GTACTCCAGC CTGGGCAACA GAGCAAGACC CTGTCTCAAA AATATATATA 1200
GGCTGGGCGT GATGGCTTAT GCCTGTAATC CCAGCACTTT GGGAGGCTGA AGCAGGCGGA 1260
TCACTTGAGG 1270
|
