| Tag | Content |
|---|
EnhancerAtlas ID | HS080-00978 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr1:43750100-43751110 |
Target genes | | Number: 14 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Klf12 | MA0742.1 | chr1:43750480-43750495 | GGCCACGCCCTCCTC | + | 6.74 | | SP4 | MA0685.1 | chr1:43750478-43750495 | CTGGCCACGCCCTCCTC | + | 6.06 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_29457 | chr1:43748843-43752786 | Fetal_Intestine_Large | | SE_31961 | chr1:43749328-43752683 | Gastric |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CCCCAACCTC CTCACATCCA ACCTGGTATC AATCCCCATC ATGTCTTCCA CTAAACATCT 60
CTGGAATGAC AATACCCTCT TCTCCACCCC ACTGCCACAG CTGAGTCCAA GCCACCTTCC 120
TCTTGTACTC TAGCCATAAT CTCCTAACTG GGCTCCCCAC CTCTGGTCTC TTCCACAGAG 180
TGATGGGCCT ACAACCCAAA TCTGACCCCA TCACTAGCCT GGTTAAAATC CCTTCAAAAG 240
CTCCCCATGC CCCACAGTGC CTTGCAATCC AGCACACGGC CCTCAAGCCA AACTCTTCTT 300
CCTCTTCTCC ACAGTTCCCT CCCCAGCACT TCAGACAGAC ACACATGCCC TCCTCCCACT 360
CACCCACCCT CCTGCTCCCT GGCCACGCCC TCCTCAGTTT TTGGGGCGCC AGTCTGTCAA 420
GGCCAAATCA GACCATACCT GCCTGTGAGG TTGTCCCTGG ACCTACCCTG GATGACCTGT 480
CACCATCCTG CCCAGTCAAC CACCAGTCAG AACCAGTCAT TGCTAGGCGG GCAGCTCCCC 540
GTGGGCAACG GCTGGCTGAA GGATCTGTAC CCTGGCGCTG CAGGGAGCTG GGCGTTCAGC 600
CCCTCAGTGT GGTGCTTGTG AAATTAACGA GGGGAGCGTG AGAGTGAATA TACAGGTGGG 660
AGCGGGAGAG ACGTCCTGGG AAGGAGAGGT CAGCTGCTCA TTCATTCCTC AGCCTGCTGT 720
GGGCCTCATC CTAGTACTAG GTCCGCAAAA CATGAGAATG TGTTACACTG GAATGAACTG 780
AATTCAATTT GACGTTTCTA AGGTTGTATT CCTATTCCTT TCCTCCCTGC CCTGTGAATT 840
CTTCCCAAGA AGACACACAC ACACTAACCT TCCAAGGGTG CATATACACT CCCCAACAGG 900
CCTCTGAACT CACAGCCCAC ACTGATCTGC CCATCCCCCA TACGCACAGC CCCTCCCCCC 960
AGGTCACACT TTCCTCCACC AACAAACACC CCTCTGACAT GCACAGACAC 1010
|
