| Tag | Content |
|---|
EnhancerAtlas ID | HS182-11124 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:18420670-18422110 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HNF4G | MA0484.1 | chr19:18421495-18421510 | TGGCCTTTGCCCCCG | - | 6.29 | | KLF5 | MA0599.1 | chr19:18421444-18421454 | GCCCCGCCCC | + | 6.02 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_24690 | chr19:18418803-18423834 | Colon_Crypt_3 | | SE_52990 | chr19:18413901-18423828 | Small_Intestine |
|
| | 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 |
| GH19I018309 | chr19 | 18420357 | 18423714 |
|
Enhancer Sequence | CCTGCGGAGA AGGGGAGCAG GTTATTAACT TACCACCGGG CCGTCTGGCC CAGCCCTGGG 60
AGCGCGGGAG GCCCTGCAGA TCCTGCCCAG CCTGCACCCC GTACCACCCC TGCAAGCTGC 120
ACAGTATCAG TCCCGGGACA TACGTGGCAA AGGGTCCACC CTGCAGGCAG GATCTGTCCT 180
GACCCCAGGC AATCCTTCAC CCAGGAGCAA GGGTGGGTGT GGTAGGCGCA GCCCCCATTG 240
TGCACTCACA AGGAAGACTG GCTCCTATCC TCTGCCCGTG GGCCTGGCTC AGGAGTGGCT 300
GACTGGGGCT CCCTCCAGCC TGGGATGGGG CTCTCTCTGG TTGGGGTTCT TCACCTGCAG 360
CCCAAAGCCC AGAGCGGGTG GGGGCCTCCC TGTGCACCAG ACACAGCCGA AGCCCAGCTA 420
CTCCTCCTCC TGCCCCAGCC CCACCTCACT TCTGGAAGCC TCTCTACATG CCCTGACTCA 480
TTCATTCATC TAAGTATCTC CTGACAGGGC CTGCGCTGGG TGCAGGGACA TGCGAGCAAG 540
CTACAGGCCT AGTGTGGTGG GTGAAGAGGG GCGGGAAATG GGGGGACTTG GGTCCTGCCA 600
GGGTGGCTCA AGGGCGGCTC CCAGCGATGC CAGTTTTAGG AGAGCTAACC AAGACTGGAG 660
AAATGGGGGC CTTGCAAAGA CACAGACTCA TGCTGCAATG CCTCCGAGGC CCCCACTGGG 720
ACAGATCGAG GGATTAGCAG GGGCCAGGGC CATTCCTACC ATATCAGTTT CCCAGCCCCG 780
CCCCACCGCC CAGGTTCCTG GACAGACCCA CGCACGACGC CTGGATGGCC TTTGCCCCCG 840
ATGCCCTTTA AAGTCAGATC ACAGTATGTT CCAGCTTGGA ACCCACCCAG GGCCCCCTCC 900
AGCCTGGGGG CAAGGTCTAA GAACCTCAGC AGGGCTCTCT AGGGCCCGAG ATCCTGCCCC 960
GCCCTGGCGG TCCTCTCCCA GCCCGACGAC ACTCCCTCCA GATGGAACTT TCTGTTTCCG 1020
GAACACACGC CATGGGCTTG CCCCCAGAAC TTTGCACGTG GTTTTCCCAC TTCTCATCTG 1080
GCTAACTTTG ACCCCAAAAG GCCTTACCTG CCCGAATCCC CAAGTCCTCC TGTCAGACAC 1140
TCTCCTCCAC ACCTGGGTAG GTGTGGCCTG GCCTAGCGCT GGGCGGGGAG GAACAGCCCC 1200
TTTGGGTGCT CACTCTCCCA GGAACCCCTC GAGGGCTCGT GGGGCGGACA CACCATGGTT 1260
CTGTGGGGAC TCAGGGCCTG GGCAGGTGAC TTGGCGCCCA GCTCTCCCAG GCAGGGCCCA 1320
GAGGCTTCCT CGTGCAGGAA CCTGGGCAGG GCCTGAGCTC ACTGCAGGGA GGCCCCTGCC 1380
TCCTGCCCAC AGCGCTCCAG AGGTCTCTCA GCCCGGGGTC TCTGCATCCT GCGGCCTGCC 1440
|
