| Tag | Content |
|---|
EnhancerAtlas ID | HS176-33173 |
Organism | Homo sapiens |
Tissue/cell | SK-N-SH |
Coordinate | chr5:149437160-149439200 |
Target genes | | Number: 11 | Name | Ensembl ID |
|
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr5:149437174-149437189 | GGGGGGCAGAGGTCA | + | 7.12 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_09705 | chr5:149434523-149449301 | CD14 | | SE_46022 | chr5:149436874-149439329 | Osteoblasts | | SE_55727 | chr5:149435688-149439759 | u87 | | SE_67531 | chr5:149435688-149439759 | u87 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr5 | 149438363 | 149438641 | | chr5 | 149437212 | 149438133 | | chr5 | 149438161 | 149438639 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH05I150057 | chr5 | 149437395 | 149439565 |
|
Enhancer Sequence | TAGGAGAGAG GGTTGGGGGG CAGAGGTCAC TCATCATCAC TGCACTGCTC AGCTCAGGCC 60
TTGACCACCC ACCACCCCAT GGTCAACTGG AACCTCCCTT TCTGATAAGA AACCCTCCTG 120
CCACACTCCA TCTGAGTGAG CATTGGTCTC TGCTCGGCTG TCCCCGGTGA GGGAGCTTAC 180
AACCCATTCT GGTTTTGGGC AGCTCTGCCT GTGAGAAAGT TCTTCACTGT TCCTAATGCC 240
AATCTACCCC TGAGATTTTC CTCCTAGCCC CTGCTCTACC CTCAAGGGCC ACAGAGAAGT 300
TGGAGTCCTC TTCCCCATAA CAGCCCTACT AGAATTGGGG CATATTCTAG GGCCCCTTGT 360
GCCCTCTCTT CTCTGGACAG TGCCTCACAC CCCTGGCTTC ACATTAAAAT CACTTCGGGA 420
GCTTTTAGGA TCAGGCTAAT TACTAATACT TCAGAAACTC TAGGGACAAA ACAGTCATTC 480
ACAGATTTAA ATCTCCCCAG GTGATCACAA AGTACAGCCT AAGCTGAGGC CCACTGGTCT 540
AGAGCAGTGC TGCTTACGCT GCAACTCATG TGCAGATAAA TCACCCCGGG AATCTCTGCA 600
ATGCAGATTT TGAATCAGCA GGCCTGGGTG GATGGGCCTG AGGTGGTGCA CTTCCAACAG 660
TCCTCAAGAG ATGCCTATGA GAGCACACTT GGGGTAGAGA ATTTGAGAAG CACTACTGTA 720
GACTGAAGCA CTACTGCTCC TAACGTTCCA GCCAGATAGG ATTTCTCTCT CCCTCCTGTC 780
CCCTCTGCGC TAGAGATGTG TACCTTGACA ATGTCCATAT TCTAGTGTTC CCAGAAGGAG 840
AAACCGAAAA AACCTTCCGC TCCCTTGTAG AAACTATGCT TCCGTTAACA GCCTGGAATC 900
CTTTGACAGA GTTGGTTTAC AGGCCATTTG CCCTCGAAAT TACCCACTCT GGGAATACTT 960
TCCCCATCTG CGTATTTGAA GATGGAAGCT AATACTTTCC TTTGGTGCTC ATTTTGATCT 1020
GATCTTCAGA GGCCTAGTGT GTGCCACCCT CATAGAAGTG TCAGGGAATC AGAAGAGGAA 1080
GTGATGCTGC CAGGCCCCCA TTTTTAAGGC CCTGGGTGAA GAGATGGCCT CCTTCTCTTT 1140
TGCCTCCCCA GGCGTGGCAG CTGACAGTAT CTAGGATGAG GGCGCAGTGT ACACCCTTCT 1200
TGTTCTGATC CTGTCCTGAC CCCACAAGCC CCTGAGACAG AGACCTCCAG GACAGCAGTG 1260
TGGCTTGGGT GACTCCTGGA CTGGAAGTCA AGAGAGCAGG ATTCTAGTCC AGGCTCCACC 1320
TCTAACCCTG ACTCATGTGT GACATGAATC TCCCCACTTC CTCTCTTTGG TTCCCCATGT 1380
GGCTCTGTCT GTTGGATGGC TCTGTTCTGG ATGGCTTCCA GGAATCACAG CAACAGGACA 1440
ACAGAGCCAT CTCTCTTTTT TTTTGAGACG GAGTTTCATT CTTGTTGCCC AGGCTGGAGT 1500
GCAATGGTGT GATCTCAGCT CACAGCAACC TCTGCCTCCT GGGTTCAAGC AATTCTCCCG 1560
CCTCAGCCTC CCGAGTAGCT GGGATTATAG GCATGCGCCA CCACGCCCGG CTAATTTTGT 1620
ATATTTAATA GAGACGGGGT TTCACCTTGT TGGTAAGGCT GGTCTCGAAC TCCCATCCTC 1680
AGGTGATCTG CCCGCCTCAG CCTCCCAAAG TGCTGGGATT ACAGGCATGA GCCACTGCAC 1740
CCGGCCACAT CTGCCCATCT CTTACTAGGG CTCCAGGCAC AGATCTTGGT TGATCTTTTA 1800
CACACACTGG GTGGTGATTT CATTGATGCA TATCTCCACC AGATTATGAG CTGCCCATCT 1860
TTGCCCTCCA CACTCCCAGA ACACGGTAGG TGTTCAAATA TTTGTTGAAT GAAGGGGAAA 1920
AGGAGTAGAG AAACAAGAGA TGGCCATAAA ACCTGTGGTG GCTACTTCCC ATGACACAGG 1980
TGGCAGGTGA GGGCTGCATA GCCACCCATT CATGAGCCAT CCAACCCTGA GCTGGCTTTG 2040
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