| Tag | Content |
|---|
EnhancerAtlas ID | HS176-18174 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr18:55880590-55881950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr18:55881863-55881883 | TGTGTGTGTGTGTTTTGTTG | - | 6.14 |
|
| | Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
| SE_27800 | chr18:55878027-55884317 | Fetal_Intestine | | SE_28643 | chr18:55877783-55884394 | Fetal_Intestine_Large | | SE_36102 | chr18:55880005-55882192 | HMEC | | SE_41571 | chr18:55880626-55881613 | LNCaP | | SE_46558 | chr18:55879702-55883977 | Osteoblasts | | SE_56455 | chr18:55879664-55882154 | u87 | | SE_59269 | chr18:55878494-55899926 | Ly3 | | SE_64353 | chr18:55879884-55882106 | NHEK |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr18 | 55880754 | 55881007 | | chr18 | 55881305 | 55881780 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH18I058210 | chr18 | 55878166 | 55884140 |
|
Enhancer Sequence | GACTGTTTGT ACCATGTAAT ATTATGAGAG AACTAGAGCT GTATGAGAGT TGGCTGTGGA 60
GGAATTTCTA TGAGAACTTG ATGAATGAGA AGCAATGTGT AGAAAAATGT ATAATATCCA 120
GTTCTAAAAG ACGCATTCCT CCTGTGCCCA TATGTGTAAA TGTGTGAGTG TGGAGAACAA 180
GATGAAAATG CTCATTCTGT ATGTTAAGCA GGGAGTGGGG TGGAGGTTAA TGTGGAATGG 240
TGGGAGAGTG GGGTGGCAGG GATTTCCAAG TCACTCACCA GTGATGAGTG TTAACCACAT 300
CCCCATTTTT TTCCTATGAA GGAAGCTGCA ATGCTGTGGT TTGAGGTTAA ACATGCTGGC 360
TCCTTCTCTT AGGTCTTGAT TTGGTTTTTG TTGTTGTTGT TTTTTTTTTA ATTCTAGTCT 420
GTTCTTGTTT TGCTGTGCTG ATATCCTCTT AGATTTTACG AGCATATTAA TTGTGAGTAT 480
TTAACATTCT TCTTTGGTTT ATTCTGAGAC CCCGTTTGCC TGCCCTTTGG CATCATTGGC 540
AGTTTTTGGT GGTCTACTGG TCTTCCTGTT TGTGCCTCTC GTTTGCCCCT TTTTCACTGG 600
AATGTGCCAG GTTGAAGCAA TATGTAGGGC CCGGTGGGAT GGGCCAGGAG GTGGCCTTTC 660
AGATGTGGCT CCTGCATGGC CCTGCTTGCT CTCTTGAGCT GCCTGCACTT CAGTCTTAGG 720
ACCACATTCC TGCTTTGGCC TACATGAAGT GCAAGGTAGC AGTGGGAAAA GCAGAGAGGA 780
AATGAAGCTT CCTGATAAAT CACCTGATCG CTGCCCCAGG GTTAGTCACT CTAGCCCCCT 840
TGGATCTCTT GACTCCATCT CTTGATTTGT TTCTTTTGAA TTTCTGGCAT CTGGAGAATA 900
CTTGTACAGC AGCAGTCCCC TGGTTTTGTT TTTCTTTCAA CCCAAGCCCA TCCCATATCT 960
GTTCATGTGA TGATACTGTG TCTTATTTTC CCAAGATTCT TATGACTGTG ATATTTAGTC 1020
TGAATCAGAG AAAGAGAGAG ATAGAAATGT ACACTCAGAG GGCCACTTGG ATGGAAACTT 1080
CTGTTGATCT CTCCAAGCCT TAGTGGGATC ATCTGTAGAG CAGGGATAAT AACAGCGCCT 1140
ATCTGTTACT GTTAGGGTTA CTGCAAAGAT TAAAATAGGT GGTGCTCTTA AAAGACTTAG 1200
AACAGTGCTG TCATATAGTA AGGATTCCAT AAACATTAGC TGCTCGGTTT GTGTGTGTGT 1260
GTGTGTGTGT GTGTGTGTGT GTGTGTTTTG TTGTTGTTGT TGTTTTAAAC GGGATCATGC 1320
TGGAAATGAT AGATTGCAAC AGAGCTTTGG GGTTTTTTCT 1360
|
