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

TagContent
EnhancerAtlas ID
HS182-12598 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr2:99079590-99084130 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12617721chr299083892hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr2:99083576-99083594GAGAGGAAGGAAGGGAGC+6.09
FOSMA0476.1chr2:99082903-99082914AATGAGTCACC-6.02
Nr2f6(var.2)MA0728.1chr2:99082727-99082742TGAACTCTTGACCTC-7.64
RARAMA0729.1chr2:99082724-99082742TCTTGAACTCTTGACCTC-6.45
RREB1MA0073.1chr2:99083675-99083695AAGCGGGGGGTGGTTGGGGG-6.62
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_09236chr2:99079158-99084603CD14
SE_12066chr2:99079319-99084532CD3
SE_14904chr2:99079467-99083737CD4_Memory_Primary_7pool
SE_15794chr2:99079364-99083484CD4_Memory_Primary_8pool
SE_16648chr2:99079378-99084411CD4_Naive_Primary_8pool
SE_17250chr2:99079662-99084190CD4p_CD225int_CD127p_Tmem
SE_17594chr2:99079277-99085843CD4p_CD25-_CD45RAp_Naive
SE_18010chr2:99079280-99085912CD4p_CD25-_CD45ROp_Memory
SE_18598chr2:99079254-99085535CD4p_CD25-_Il17-_PMAstim_Th
SE_19649chr2:99079438-99084324CD4p_CD25-_Il17p_PMAstim_Th17
SE_20144chr2:99079165-99092088CD56
SE_21398chr2:99079564-99083893CD8_Memory_7pool
SE_22521chr2:99078980-99086005CD8_primiary
SE_32475chr2:99078939-99094101GM12878
SE_39553chr2:99079503-99082482Jurkat
SE_39553chr2:99082746-99084676Jurkat
SE_43508chr2:99078937-99085664MM1S
SE_50377chr2:99079480-99084237Sigmoid_Colon
SE_52736chr2:99079487-99082603Small_Intestine
SE_52736chr2:99082704-99084118Small_Intestine
SE_55432chr2:99079621-99082544Thymus
SE_55432chr2:99082626-99083275Thymus
SE_63026chr2:99060396-99125684Tonsil
SE_66467chr2:99079503-99082482Jurkat
SE_66467chr2:99082746-99084676Jurkat
SE_67159chr2:99078937-99085664MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr29907960699082526
chr29908140299081780
chr29908280499083102
chr29908381899084044
Number: 1             
IDChromosomeStartEnd
GH02I098462chr29907901299091939
Enhancer Sequence
CACCGCGCCC AGCCCACAGA CATTTTAAAC TAACCTGTAG CATCCTGAGT GAGGCTTGTC 60
AAAGCTGCTT TTGACCCCAG TTTCAGGTAC ATTGGCTCTG TTGGGCTTTC CTCTGCCTGG 120
CCTATCAAGC GGCCAACTCA AGCTGCAGGT GCAAGGGCAG ATGGTTCTGC AGGGACCTTA 180
ATGACAGCCA GGCCCAGGAA CACACAGTGC TTGTGTGGAA GTCTACATTT CAGCTGTGAT 240
GGTGTCTCGC TGAGGCTGGT TCTGGCCATG CCCTCCCAGC ATTTCAGCTG TTCCAACCAA 300
GGTGCTCTAC ATCTCAGAGG GAAGGCAACG GCCTGGGCAG CACGTTGCAC GTACATTTTG 360
GAGTCATGTT GGTTGGTGGT CTTCAGTTTC TGAATCTGTG ATATGGCATG GTCATTCATC 420
ACAGGCGAGG TGATGCAAAG TTACCAACTG GGAGCACACC TGCCCCTTCT CATTCACTCA 480
CGCAGCAGGT AGTTTTCAGG CACAAAGGAA TTGACTTGTG GAGCTGGCCC TGGGGTCTGT 540
CTGTAGGAGA GCAGGAAGTA GTAGCCACCT GCGGAGGGCT CACAGGCATG TGCCTGCGAG 600
ACTGCTTACA AGCCCCTGTG CGGGATTTAG GGCAGACCAG AGCCATGAGC GTCCATGGTC 660
AAGTGAAGGT CTGGTAGGTG TGAGCTGTTA GCCCTAGGGT CTGCTGCATG CGGTGCCAGG 720
GGCTGAGGAA TGCTGAGGCA GCTTTTCCTC CAGTCTCTGC TCGCTCCGTG CACAGCCCTT 780
GTCTCCTGCC TGATAGTGGT CAGTAGTCAG TTGGCTTAGG GTACACGGTC TCCACCCAGT 840
GAACCTGGCG CTGGCAGAAG CTTGTAGAAG AATGGGTGCA AAAAAGATAT CTCAGAGGGC 900
CTGCAGATGG CTGTTTTTAG GAAGTGAATA GGCTTCTTCT TTTTCTTCAT TTTTTCTTTA 960
AGATACTCTT GAGGTTTTGA GGCTCCACCC TGAGCTCTTT GTGGCTGAGG GCTGCTGTGG 1020
CTTGATGAAG GGGACAGTCT TCAAATCTTG CACAGGCTGG GGAAGGTTGG GACAGCACAG 1080
CCCTGAGTCT CGAACAAAAT GGGGCAGAGG GGAGGGCAGG AGAGCCGTCA GATTCATGGG 1140
GCCACATCCT CGCAGCAACC CAGGGGAAGC TGAGGCCCCA GGGTCTGCAT GATGGAGGCC 1200
GAGCACGACG GAGGAAGTGG AATTATTGCA CATGGTGGGT TTCGACACTT GGGACTCGCT 1260
CCTCAAAGAG GAAAATCGAG AGTGGGGGTG CACAGAGCAA GGGCTGAAGA AACAAAAAGC 1320
AGGGGGTTTA GGGGAGAGAT AAACCTCTTT GCATGAGTCA AGCTGAAAAG CAGTTTGGAA 1380
GGTCAAGTGC TAGCCAGTGT CTTTTTTTGC CTGCCCAGCC TCTTCTTCTG CCATGTCTGC 1440
CCTGACAGGG GCAGAGTTCT CAGTTCCCAT GTCAGAACTC GGCACCAGCT TCTCTGTTGA 1500
CAGTTGCAAG GCCTGTGGCT GAGAGAAGTA CTTGTGCTGT GTTTCTGCAA GGTAAGATGG 1560
CCCTGATCAC AGCTCATGAT GCCTGAGATC AGGAGGGTCT GCTCCATGAG ATATCAGCAG 1620
AGGCCATCCT GTGAAATATT TTAACTAATT GAACTGAATG TTGAAGACAA GGCCTGTGGC 1680
AGTGTTGTAT TTATATGTGA CAAGCCGAGA GTCCTTGGAC AACCTTGGAA ACTCCTTTTT 1740
AGGACAGAAT CAACTGAGAC GATACACACG AAGGAGCTTT TGTGAGCAGA GTACAGAGCT 1800
CGTTATTGCA GTACAAGGTT GTAGGTTTTC ACACAGCTTT TGAGGATGGG TTGGTGGCCC 1860
AGGGAGGATG TCAGGAACTG TCCTTCACTA ATGGGGATTC TCGAGTTCCT ACCACGTGCC 1920
AGATAGCGTG CTGATTGCTT TGTATCCACT TCCCTTTTAA TCCCTTGTAT TAGCTTCCTG 1980
TGGTTGCTGT AACAAACTCG GTGGCTTAAA GCGAAAGGAA CTTATTCTCT CACTGTTCTG 2040
GCCTCCAGAA TCACTGGGCT GAATCAAGCT GTGGGCAAGG CCATGTTCCC TCCAGTAGCT 2100
TAGGGCGGAA TCCATTCTGT GGCTGCTGGC TTGCCTCGGC TGCCGGCCCC TTCCTCATCT 2160
TCACACCAGC AGGGTAACAT CTTCTCTCCG TGACTCCGCT TCTCTCTGCT TCTGTCACAC 2220
GGCCCTCTCT TCTCTCCGAA ATCTCCTGCC TTCATATAAG GACATTTGTG ATGGCATTTG 2280
GGGCCTACCA GTGTAATCTA GGATAATCTC ATCTCAAGAT TCGAAACTTA ATTGAGTCTG 2340
CAAATCCTTT GCTGTATAAG GTAACATTAA TAGGTTCCAA GGATTTGAAC GTGAACCTCT 2400
TTTGCAGGGG GCATTATTTG ACCTGCCATA CCTCACAGCA GCCTGATGAG GACCATACTG 2460
TCCCACATAC AGTGGGCTTA ATGAGGAAGC TGAGGCTTGG GGAGGCCTAG GGGTGGCCAT 2520
GGTCCTTTCC TCTCCCAGAC TCTGGGGTAG CTGACTCTGG GGTCATTTTG TCATGTTGCT 2580
GGGCACTCAC TTGGTGAACA GATAATCCCC TGTCATTTTA CTATGTTGTT ACATGGGTTT 2640
GAAAAAAGAG TTTTTCAACT CTCTGGCTGA GCCCCTGTTC CTGTGAGGGC CTGTGGTTTT 2700
TCCTCCCGGC TCCACCCTGG TTTCGGCGCA GTACTTGAGC AGACGGTGGC TTGGGTCTCA 2760
CTCTAGCGCC CTCCCCCTTC CTCTCTGGCT GTGTGCCCAG GCTGGCCCTG CCCACCTTGC 2820
TCAGTCTCTG CTCCATCTGC CACAAGTCTC ACTCCAGCCC TCCCCCCAGT AGCTTAGGAA 2880
GGGACCTTCT TGTTACGTTT TTTGTTTTGT TTTGTTTTTT GTTTTTTTGT TTTTTTGAGA 2940
TGGAGTCTCA CTCTGTTGCC CAGGCTGGAA TGCAGTGGCG TGATCTCTGC TCACTGCAAC 3000
CTCTGTCTCC TGGATTCAAG CGATTCTCCT GCCTCAGCCT CTTGAGTAGC TGGGACTACA 3060
GGCGTACGCC ACCATGCACA GCTAATTTTT GTATTTTTAA TAGAGATGGG GTTTCACCAT 3120
GTTGGCCAGG TTGGTCTTGA ACTCTTGACC TCAAGCAATC TGCCCGCCTT GGCCTTCCAA 3180
AGTGCTGGGA TTACAGGCGT GAGCCACCGT GCCCGGCCTT GTTATGTTTT TTAAGCTAAC 3240
CCTGTAGAGC ACTCACTGTG CACCAGCACC TGTTGGCTCA AGGGGGTGAC AGACATTCCC 3300
TATCACAGAT TACAATGAGT CACCGGCATT TTTGGAATTT CACTAAGCGT CGTTGCTGTG 3360
CTGTGCCTCA GCATGCAGCA CTTCATTTAA TCCTCTGGAC ACCTTGAATG ATAAGTGTCT 3420
GTCATCCCAT TTTACCCGTG AGAGAATTGC GGCTCAGAGA AGTTGTCACC CAGCTGGTTG 3480
GTGGCAGAGG TTTCAGAGGT CTTTCTGTGC ATAAAACCCT CACTTATGGT TATGCCAGGT 3540
AGGCCTTGGA GGGGATAGAC CCATCGCCAA ACTCACAGGA GAGAGAGGAG GGCACTCACA 3600
GGTGATGATG TCTATCTGTC TTCTTTCTGG TGGGGACCCA GAGTTTTATT TCCATCTCGT 3660
TTTCTTTATG AATGCTTGTC TCACACTTAT GTATTTTTTG GGCAGTCCCT GAATAACTAC 3720
ACCAGGCTTC TGAATGCCGA GTTTCTTAGA GTAGCCGGGA AAGGGCCTTT TTCTTTTCCT 3780
CTTGGATGTT CTCTTAGTCT GTTTTGTGCT GCTATAAAAG AATACCTGAG GCTGGGTAGT 3840
TTTTAAAGAA AAGAGGTTTA CTTGGCTCAC AATTCTGATG GCTGGAAGGT TCAAGACTGG 3900
ACATCTGCAT CTGGTGAGGC CTCAGGCTGC TTCTACTCGT GGTGGAAGGT GAAGGGGAGC 3960
TGTCGTGTGC TGAGCTCACA TGGCGAGAGA GGAAGGAAGG GAGCGGGTGG TGGTGGTGGT 4020
GTCCCAGGCT CTTTTCACAG CCAGCTCTTG TGGGAACCAA CGGAGTGAGA ACTCACGCAC 4080
CCTCAAAGCG GGGGGTGGTT GGGGGAGGGC ATTAATGTAT ACATGAGGGA TCTGCCCCCA 4140
TGACCCAAAT ACTTCCCATT AGGCCCCACT TCTGACATTC GGGATTAAAT TTCAGTGTGG 4200
AGTTTGGAGG GGACAAACAT TGTCCTCTTG TGCCTGTGCC ACACTTGCCC CTCCGTCCCC 4260
CTCATCTGCT GATGATTCAT CACACTGTTA ACTTGGTCTC TACATCTGTT TAAACGCTTT 4320
CTCCTTTCCC CTATTATGTT GCTGTTAAGA CTGTGAAGCT GTCAGCAATG TTAGCGACAC 4380
CGTCCACATG TGGGGACAAC AGGTCCAGTG AACCTAGCAT CATCAGTGTC CTTTGCCCTT 4440
GGAACTGAGT GGAAATTATC TTCTCAGCCT CCATGGATTT AACTTCTGTG TTCTTGATGT 4500
GAAGCTTCTT TTCCTTAAGT TAGAGTTTTT GCATATACAT 4540