| Tag | Content |
|---|
EnhancerAtlas ID | HS182-00296 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr1:16515150-16516100 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF4 | MA0039.3 | chr1:16515443-16515454 | CCACACCCTGC | + | 6.62 |
|
| | Number of super-enhancer constituents: 13 | ID | Coordinate | Tissue/cell |
| SE_23091 | chr1:16515057-16516232 | Colon_Crypt_1 | | SE_23751 | chr1:16515130-16516087 | Colon_Crypt_2 | | SE_24743 | chr1:16515648-16516115 | Colon_Crypt_3 | | SE_26540 | chr1:16513910-16517815 | Esophagus | | SE_28102 | chr1:16515172-16516184 | Fetal_Intestine | | SE_29455 | chr1:16515096-16516063 | Fetal_Intestine_Large | | SE_31527 | chr1:16515204-16516074 | Gastric | | SE_34268 | chr1:16514127-16516193 | HCT-116 | | SE_34628 | chr1:16513819-16517068 | HeLa | | SE_36144 | chr1:16514154-16516161 | HMEC | | SE_50427 | chr1:16514084-16516281 | Sigmoid_Colon | | SE_52536 | chr1:16514970-16516287 | Small_Intestine | | SE_64726 | chr1:16514111-16515805 | NHEK |
|
| | 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 |
| GH01I016187 | chr1 | 16513841 | 16516098 |
|
Enhancer Sequence | GCTATTAAAA GACCTAACAC CTGGCACTTG GGTTGGAGAG AATAACATGG CTGTCGTTAT 60
ATACTAATCC TTGGCCAGTC TGTCCTGGGA GATCAACTCC CCTTTGCATA GGGCTTTTTC 120
GAAGTCCTTT TCCAAGGCAT CACCTTCTTG TAGCTGCATT ATCATGCCCG TTTACCAGAT 180
GAGGAAACTG AGGCTCAGAG AGGGGAAGCA GCTTGCCTAG AGCATCGTGG CTTATAAGTT 240
AAAGCAAGAC TCAAGCCAGG TCCACCTGCC TCCAAACCCG GTGCTGGACT TTCCCACACC 300
CTGCTTTGGA AACTCTAAGG AACCTTCCAA TCCCCCAAAT CCTATTGCCT CATTTAAGTA 360
AAGCAGGCCT GGTTTCTGCC TCCTTCAGTG CCCCTCTTCT CCTCCCACAC CCTTCCAGCA 420
GCCGAAACGC TAGACCCAAT AGCTTACCCC TTCCTCCTTC CTGACCAGCT CCCAACCCTC 480
AGGGCAGCTC ATGAGCCAAG AGCTTGAGAG TGGCTTCCAA AGGTCATCCT CTCCACCCCG 540
CTGTGCCCCA CCCAAGCAGA TGACTGTTCA TCCTGTTCTT CACGCTGCTC AGGGGAAGAA 600
ATTCCCCAGC TTCACTCCCT CCACTCGCCC AGGTGTCTGA GACAGTTCCC ACAGTTGGCA 660
AACTCTGCCT TAAGTCCCAC CAGAGTCCCT CCTGCTACAA CGTCAGCCCA TTTATTTTAG 720
TTCTTTCTCC CAGTAGCATC AGAAATACAA TCTGGGGGGA GACAAACGCC GGGAGAGTGG 780
GATCCTGGGA AGGGGAAGGC ACACTTGGGG ACAGGAAGTG AGAGCAAACC CAGGTTCAAA 840
TCCCGGTCAG GGTGACAAGA GTGGCCAAGC GAGGCCAGGC GCAGTGGTTC ACACCTGTAA 900
TCTTAGCACT CTGGGAGGCT GAGGGGGGCA GATCACTTGA GGTCAGAAGT 950
|
