| Tag | Content |
|---|
EnhancerAtlas ID | HS113-01031 |
Organism | Homo sapiens |
Tissue/cell | Keratinocyte |
Coordinate | chr1:43749600-43751110 |
Target genes | | Number: 25 | 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 | CCTGGCCCTT CTAAGTTGAA AGCCGCTGCT GCCCACCTCT ACCCTCAGCC CTTCAAGCAA 60
ACCCCTGTCC TTTCACCTCT ACTCAAAGGA GGCCCACACT CTGCCCCCAC AGGGAGGCTC 120
AAGCCAGGGA GTATCCAAAT GAGGATCACC TGAATCAGGA AATTATCACC CAGGGCTGGG 180
GACACCTAGA GGAGGAACAC TTCAATTAGG GGAGTAGCTG GAGGAAGATC ATCCAGGCAT 240
GGAAACACCT GTAGGAGGAG CACCTGGATC AAAGGAGTGT CTGGAGGAGG CGCACCTGAA 300
TCTGGGGAGT ATCTAGAGGA GGAGCATGAA AGTTAGAAGT ACCTGGCAGA CGAACAGCTA 360
GGGCAGGAGC ATATCTGCCA GTGGAGCACC TGAACCAGGG GAGTCCTTGG GGGCAGAGTA 420
GCCGGGCTAG GGAAGTACTT AGGAGAGAAG TTGAGGGGAG TACCCCAGTA TATTCTTTGA 480
TACAAGTGCC TTCAAACCCC CCCCAACCTC CTCACATCCA ACCTGGTATC AATCCCCATC 540
ATGTCTTCCA CTAAACATCT CTGGAATGAC AATACCCTCT TCTCCACCCC ACTGCCACAG 600
CTGAGTCCAA GCCACCTTCC TCTTGTACTC TAGCCATAAT CTCCTAACTG GGCTCCCCAC 660
CTCTGGTCTC TTCCACAGAG TGATGGGCCT ACAACCCAAA TCTGACCCCA TCACTAGCCT 720
GGTTAAAATC CCTTCAAAAG CTCCCCATGC CCCACAGTGC CTTGCAATCC AGCACACGGC 780
CCTCAAGCCA AACTCTTCTT CCTCTTCTCC ACAGTTCCCT CCCCAGCACT TCAGACAGAC 840
ACACATGCCC TCCTCCCACT CACCCACCCT CCTGCTCCCT GGCCACGCCC TCCTCAGTTT 900
TTGGGGCGCC AGTCTGTCAA GGCCAAATCA GACCATACCT GCCTGTGAGG TTGTCCCTGG 960
ACCTACCCTG GATGACCTGT CACCATCCTG CCCAGTCAAC CACCAGTCAG AACCAGTCAT 1020
TGCTAGGCGG GCAGCTCCCC GTGGGCAACG GCTGGCTGAA GGATCTGTAC CCTGGCGCTG 1080
CAGGGAGCTG GGCGTTCAGC CCCTCAGTGT GGTGCTTGTG AAATTAACGA GGGGAGCGTG 1140
AGAGTGAATA TACAGGTGGG AGCGGGAGAG ACGTCCTGGG AAGGAGAGGT CAGCTGCTCA 1200
TTCATTCCTC AGCCTGCTGT GGGCCTCATC CTAGTACTAG GTCCGCAAAA CATGAGAATG 1260
TGTTACACTG GAATGAACTG AATTCAATTT GACGTTTCTA AGGTTGTATT CCTATTCCTT 1320
TCCTCCCTGC CCTGTGAATT CTTCCCAAGA AGACACACAC ACACTAACCT TCCAAGGGTG 1380
CATATACACT CCCCAACAGG CCTCTGAACT CACAGCCCAC ACTGATCTGC CCATCCCCCA 1440
TACGCACAGC CCCTCCCCCC AGGTCACACT TTCCTCCACC AACAAACACC CCTCTGACAT 1500
GCACAGACAC 1510
|
