| Tag | Content |
|---|
EnhancerAtlas ID | HS047-32234 |
Organism | Homo sapiens |
Tissue/cell | Fetal_placenta |
Coordinate | chr8:11843530-11844800 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr8:11843949-11843967 | CAGGGAGGGGCGTGGCCT | - | 6.51 | | KLF14 | MA0740.1 | chr8:11843952-11843966 | GGAGGGGCGTGGCC | - | 6.25 | | SP1 | MA0079.4 | chr8:11843953-11843968 | GAGGGGCGTGGCCTG | - | 6.62 | | SP3 | MA0746.2 | chr8:11843953-11843966 | GAGGGGCGTGGCC | - | 6.18 | | SP4 | MA0685.1 | chr8:11843951-11843968 | GGGAGGGGCGTGGCCTG | - | 6.64 |
|
| | 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 |
| GH08I011986 | chr8 | 11843710 | 11844709 |
|
Enhancer Sequence | CCCACTAGGG ATCCTGAAAG TCCAGGACAC AAGGTGGGGG TGCTGGCGGG GAAGCCCTAA 60
CCCGAACTAA CGCAGGAACC GACTTGGGGA TGGTTATGGA CTATAAACTA TTCCATACTT 120
TTAGGGGGAG ACCCTTGCAT GCACTTCCAG ATCCCAGCGT AGATTAAGTG CAGCCATTCC 180
TTACTGTTCC TCACAGGAGG CCTTGCGGCC AGCTACAAAG TTCAGGCGCT GGTTGCAGTT 240
TGAAAGAATC TCCCAACGGG GTTCACAGTA CAACCTCGGT GGGGACGAAC TTCCTTGGCC 300
AGGGCCGGGG CGGGGAGGGT GAAAAGCGGG CTGCAAGTGC AGGAGCCGTA GGTGCAGAAG 360
TCGTGGGTGC AGAAACTGCA AGTGCAGGAG CCACGGGAAC ACGCCGGCTT TGCAGCGGAC 420
AGGGAGGGGC GTGGCCTGAA CGCCTGGACT GCAATCTCTG CGGGGAAAGC TTATGACTCC 480
CGGCAGCCGC GAGTTCTGAT TACAGGCTGA CAGGAACTCA GCTCGCTGCT TCCAGTGGAA 540
CACCGTGGGA GTGGATCTGC CTTGTCAAGT GGGTAGGAAC TGTGGAGCTT ACCACCGCCT 600
GCTACTCCCT ACTTCTTGCA CAGACTCTTC TGTGCAGCAG GGGCAGCAAC GCTGCCCTCT 660
GAAACATTAA CCTAGTGGCC TGAGACCCGC TCCCATCCCC CAATACCCAT AGAAGCTCCT 720
TCTTTCTCTG CACACGGAGA CCAGTGTGCA GGCCCTCCCG ACCCAGCCCC TACCTGGCTT 780
TGCCCGGCCA CCCGCCCTGG TAACTCAACG CAAAGGACAG AGTCTCCTGG GAGCGACATG 840
GCCCCGCCCA TGTCCGGAGA AACCAGAGTA TCCCCCTCTG GGCAACATCA GGCAAGCAAA 900
AATCCCAGGG CTACTACCGC AGCTGCTGCT CTTTTGCAAG CGCCACCTCC TAGCTGGAGG 960
CCAACCCACA CAGTCCTTGA CAGTATCTCC TGGTAGATTA ACATTGCACC CAGGAAGGAG 1020
AAAACCGCTA TGGGATCTCA GCTATCACTG CTGCCTGCAC CACTCTGGCT GAACAGGAGG 1080
TCCTGAGTCC GTCCACATGA CCAGTTCATT ACTACTATAA CCCGCATTCA AGAAAGCTAA 1140
CATACTAAGG CTATCAATAA CAAAGGAATT TCACAGAATC TGTGTCACAA CCTTGCCACT 1200
CCCATTAGAG CTGGTGCTGC TACCCACTGC AGGGAAACTT GAGCATAGGT CACATAACTG 1260
GATCCCTTGC 1270
|
