EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS182-22239 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr9:136370580-136372990 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs117816992chr9136371268hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
RREB1MA0073.1chr9:136371610-136371630AGTGGGGGGGTGGGTGGGGC-6.51
ZBTB18MA0698.1chr9:136371149-136371162CTTCCAGATGTGG+6.11
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9136371009136371531
Number: 2             
IDChromosomeStartEnd
GH09I133505chr9136370572136372600
GH09I133507chr9136372936136373045
Enhancer Sequence
GTGGCAGAAC AGGGCAGGAC AAAGGAGGCC GTGAGTGCAG TGTACAGCAC ACAGGACTCA 60
GAGACCCCAA ACTTGGGGCC GTGTCCTGGC TCTGTCAGTG TGAGGTCTCA CCCATGCAGA 120
CACTCCGTGG ATCCTTGGTT TTCCAGCTGG TGAGATGGGG AAGCCAAGAT GACTAAGATG 180
CATGGTGATG AGGAAGTGGT CCCAGGTGCG AGAGCCTGGT CCAGGCCTAA AGACCGTCAC 240
GGGAGTGATC TCGACAACTG GTAGGGCGAA GGCACCATGG GACCCAGCAT AGAAGAGCAG 300
GTGTCTGCAG GAGGGACAAG TGGAGCTCTG GGGCCTCTTA GGCTGCCTTC TGTGCTGACA 360
TCTTTGGTTC TGCCATTGTG GTTTCTGGAA TGGGCTGGCA GGCCAGGGGC CAGAGAACGC 420
CCCAGTTTCC TCTGCCCCTC CTCTCCTACC TCTGGAAGGC TCAGGCAGCC AGGGCCGGTG 480
GTCTGAGGCT GCAGCTTCCC GGAGCTCCAA GCCAGCAGCA GACGCTTATC AGCCTGCTGT 540
GGTGCGGGGG CCGAACTCTG CCCAAACGTC TTCCAGATGT GGCCGCAGCT ACTCGATAGC 600
CTGGCTCCAG CCGGGGCTCT AGGCCAGCAG GCTCCCGTTA GCCTAGCTGT TAGGAAAACA 660
AAACCCAATG AAGGCCCAAG GGACCCAGCT TCTCGGAAGG GAAGGGAGTG ATTGGGCAGA 720
AGCCCTGGCC AGGCCCGGCC ACTGGCCCTA AGCTTGGGGT GGTCATGGCC GTCTGCTGGC 780
TCCTCTGGGC TCCTCCTGGG GTGAGCCTGG GCCCCCTGGC TAAAGGGGTT CCCCTGTGTG 840
CAGGATGCAG CTTTTGTCTC TTTTGCTTCT CCACAGTGTG TGCGGGTGGG GGGCGTGGGG 900
TCATGTCCCT ATCACCGTAG ACAGGATGGC AGCTTGACAA CATGGTGCAG TTTGCCGATG 960
AGCCTGAGGG GCCGGTGCAC CTCTGCTGCC TTCCTGGCCC AGGGCGGGAC TGAACCCAGG 1020
CCAGGTTCTC AGTGGGGGGG TGGGTGGGGC TGGGTCCGAT GGCCCCGGCA GGATAAGCAG 1080
GTGTCACTGC TGGAAGTTTT GGGGACTGAA GGGCCTTACC CAAGGACACA CAGCCCCAGG 1140
GTGGGTACTC CAGAGCCAGT TCCTTTCTGG CTCATGGCCT GCTCCCGCCT GCGGCCGGTG 1200
TGCAGGTCAG CGGGGTCAAG GCTGTCTTCT GTGGTCACTG ACTAACTGTT TTTTGCATGT 1260
GGACTCGTCA GGGAGGCATA AACCTGCCCT TGCCAAGACA GATATGGAAA AATCCACTCA 1320
TCCATTCATT TGACAAATAT TTGTTAAGTG CCTGCCTACG GCCCGCCAGG CGGAGCGCGG 1380
GAACGCGATG CTGATTTAGA CACTCCCAGC CTGGGTCGAG CTTCCAGGCT TCATGGGACC 1440
ACATCCGCCC CTGGCCTGCT GGGCATGGTC TTGGCCTGTG TGATGCAGGC TGGGCCCTGA 1500
GCGACGGCTC TCCCGCCACC TCCGTCGTAC AAAGGCTGCA GGGGAACGAA TGACTAGGTA 1560
ACTGGGGGTG ACCTTGACTC TGTGTGGCTT TAAGACACAA GCCAGCTGTC CAAAAGCTTT 1620
GAGCTATGAT TGCTGGCAAC AATTTGCCTC AATACCCCTC CCAGACCAGG GCAGCTCCCC 1680
GCAGGCTGGG GGCCATGGCT GAGAACTGCT GGAGGGACAC ACGTCCCAGG CACCACCAGT 1740
CACCGATGAC TGGGCTTTGC ACCACTGGAA AACCAGCTGG GGGACTGGTG GGCCCCCAGT 1800
GAGCCCTGCT GATGCCACCT TCGCTCTCCC AGCGCCTCCC TCCTCCCCAC ACTCCTGCCT 1860
GGTGGACTTG GCTCCCTCCC GATGGGCAGC AGCCTTCCTG GTCTCTTTCT GCCACTGCCC 1920
ACCTCTTCAT GGAAGCCAGA CCCACTGTCA GGCTCCCCCA CCTAAAACCC TCACATCCTT 1980
AGAACCTGCC CACTGACGCC CACCTTGTGC AGTTCCCAGA CAAACCCTGT TAGATCTTTC 2040
TCCCTCTCCC TGGGCCACTG GCCCCTTCTC CTTCGGGTCT CCCAGCAGCG CCCGCACTGG 2100
GCAGCCTTTC TGACCCAGCG CCTCACTCCC CCAATCCCCC GCGATGGCTC AGTTCTGGGT 2160
CTGCCTCCCC CATCAGTCTG TGCACCATCG GAAGGCAGAG CCCAGGTCTG CTGGACTTGT 2220
GTGACTCCTT GGGGTTGGGA AAGCTGTGCG GCACATGGAG ACACTCAGGA AGGGGCGACG 2280
TTTAAACTGG GCCCTGGGAC CGAGCCCCCT GTTTCCTGCT GTTTCAGGTC AAGCGTTGGG 2340
GCGGCACAGC AAGACCAGGG CAGAGCTGGT GATATGACAC AGGGCACGAT TCACCCGAGA 2400
TGGTTGGAGG 2410