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

TagContent
EnhancerAtlas ID
HS182-06256 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr14:35866590-35868990 
TF binding sites/motifs
Number: 9             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr14:35867079-35867100GTCCAGTTTCAGTTTCTGTAA+6.37
IRF8MA0652.1chr14:35867083-35867097AGTTTCAGTTTCTG-6.14
IRF9MA0653.1chr14:35867083-35867098AGTTTCAGTTTCTGT-6.5
MecomMA0029.1chr14:35866768-35866782GGGATAAGATAATA+6.12
Nr2f6(var.2)MA0728.1chr14:35868939-35868954GAGGTCAGGAGTTCA+6.22
SPI1MA0080.4chr14:35867614-35867628CACTTCCCCTTTCT-6.22
SPIBMA0081.2chr14:35867614-35867626CACTTCCCCTTT-6.07
SREBF1MA0595.1chr14:35868658-35868668ATCACCCCAC+6.02
ZNF740MA0753.2chr14:35868194-35868207GTGGGGGGGGGGA-6.3
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00565chr14:35866191-35876369Adipose_Nuclei
SE_06617chr14:35867649-35869383Brain_Hippocampus_Middle
SE_10731chr14:35867035-35868053CD19_Primary
SE_19323chr14:35867004-35867965CD4p_CD25-_Il17p_PMAstim_Th17
SE_23298chr14:35866410-35867635Colon_Crypt_1
SE_23298chr14:35868103-35868902Colon_Crypt_1
SE_26422chr14:35866391-35868988Duodenum_Smooth_Muscle
SE_26613chr14:35866394-35868010Esophagus
SE_26613chr14:35868081-35869111Esophagus
SE_27693chr14:35866317-35869024Fetal_Intestine
SE_28626chr14:35866306-35869051Fetal_Intestine_Large
SE_30638chr14:35866757-35868050Fetal_Muscle
SE_31925chr14:35866386-35869079Gastric
SE_34831chr14:35866436-35869096HeLa
SE_41052chr14:35866454-35869024Left_Ventricle
SE_42211chr14:35866408-35867950Lung
SE_42211chr14:35868006-35869104Lung
SE_48930chr14:35866545-35868020Right_Atrium
SE_48930chr14:35868069-35869006Right_Atrium
SE_50091chr14:35866449-35869094Sigmoid_Colon
SE_52425chr14:35866359-35868984Small_Intestine
SE_53368chr14:35866670-35868023Spleen
SE_53368chr14:35868036-35869007Spleen
SE_55029chr14:35866920-35867910Stomach_Smooth_Muscle
SE_56156chr14:35866459-35868975u87
SE_62869chr14:35866439-35886616Tonsil
SE_65723chr14:35866635-35867355Pancreatic_islets
SE_65723chr14:35867764-35869321Pancreatic_islets
SE_67556chr14:35866459-35868975u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr143586816035868928
Enhancer Sequence
TGAGCCCCCG CACCTGGTCA CACTTACCTG GATTGCTGGC CGGTTTGTGG GCCTTGGCCC 60
TATTTTCATG TCAGTGTTCA GAGTCCAGTC CTACTTGTCA ATGACTCAGA TTGGCTGATG 120
CTGGGTCATA CTTCCTGCCC CCTGTGAAAA GGGTGCCTGC CACAGTCACT TGGGGCATGG 180
GATAAGATAA TATAGTACTG GCAGGTAAAT AGCTAACTGG AATATGAGCT CGGGTCCCGT 240
CTCTCCCACC TGCACTCCGC GCTGGTGCCT GGGCTCAGCT CCCGTGCTAT GGGCTTTCAT 300
CTCATCACGC CTTTCCATGC AGTTGTCTGT CTCCCTCTCC ACCTAAGCAA GGAGCTCTTA 360
GGGGCAGAGG CCATGACTTA TTCCTCTTAT TCCTGCCCTT GGCAGGAGGC CTGGAGAATA 420
GTTCTTTTTG ATGCAAATGA AGGAATGGGT TGGAGAGTCG TACTTCTCTA GGAGGGAAAC 480
ACAGGTGAGG TCCAGTTTCA GTTTCTGTAA TGCTCTCTTT CAATGGGGAA ACAGCCTAGG 540
ATATTCTTGT CCAGGCACCA GAGGTTGGGG AATGTTTCTT GGGCATGTTT CAGACTGGAG 600
TTCCACAACT CAGACTTTTC TTGCCAAATG AAATTTCAGC TACACTTAAG GCAAGTTAAT 660
GAAAATCTGG CAGAAAGCTG GGGGTGGGGG AGTGGGTGGG TACGGGGGTG GGAAGTCTTG 720
GGGAAGGAAG ACCCATCTGA CAGACTCAAT TCTGTCACCA CTTAATCACT TCCAGTAGCA 780
ACTGAACTTT CCATGCAAAT CCACCCAAGC TCCCAGCCTT CTGAATTTCC AGGCCCCAGG 840
GGAAGGTCTT CAGATTGCTC AGACTAGTTT GTTCCCTCTT TAAAGAAAAA TCCTTACTTT 900
CTGGAAGGAC TTGGTACACG TGGCCGCTAC AGGAAATGTA TCCTGATGGA TAAGGCAGGC 960
AGAAGGAATC AAGGAACTGA ATTCAAGGAA GTTGCTGATG TGATATATTA TTTCCCCCTC 1020
ATATCACTTC CCCTTTCTCT AGGCACTCTT AGTCCTACCT GTCCCCACAC AATCTGTAAC 1080
TTCTTGGAGG AAATCAAAGT GCATTAAAGA AGACTCTCCG TCTGCTGGCC TGTTTACTTT 1140
GAGATCTTTT GCTCTTGTTT GCTTAGGAAT TTGAAGATTT TCTACAGATT AGAATGTTTC 1200
CCTTCTAAAA TTTTCCTTTA GGGAACTCCA GGCTCCAGTC ACCCAACCAA CAGGCAGGAC 1260
AGAAAGATAA TAAATTTAAA ACAAAAAGAA AAGAAAAGCA GGGAGGGCTG GGTGTGGTGG 1320
GTCACACCTG TAATCCCAGG ACTGTGGGAG GCCAAGGCAG GTGGATCACT TGAGGTCAGG 1380
AGTTCGAGAC CAGCCTGGCC AACACGGCGA AACCCCATCT CCACTAAAAA TATAAAAATT 1440
AGCCGGGTGT AGTGGTGTGC ACCTGTAGTC CCAGCTACTC GGGAGGCTGA GGCAGGAGAA 1500
TTGCTTGAAC CCAGGAGGCG GAGGTTACAG TGAGCCGAGA TCATGCCACT GCACTCCAGC 1560
CTGGGCAAGA GAGTGAGACC CTATCACACA CACACAAAAA AAAGGTGGGG GGGGGGATGA 1620
GAAATGGGGA GAAGAGCTAG AGAGTAAGGA ACCGGGGCAG CCTTCAGTGC TTAACTGGGC 1680
CCAGCTACCT CGAGATTTAT GCAGATGACA GAACCTTTTC CAAGGTTTAG GACCTAGAAA 1740
GAAGAAAAGC TGAAGCCTAG AAAGGTGGGA GACTGGGCCC AAGTGGGTGA GAAGGGGCCC 1800
ACCCTTGCTT GACCATGGAG GGTGACGCCC CTATGCAAGA GCTGGGCTCT AAGGAGGCTG 1860
GGGATGAGGG GGTGGCGCAC AGCTTTGTCC TGTTTCTACA ACCTAGCACA GAACTAGAGA 1920
CAGCGTATGG GTGAATTGGC ACAAATTTAA CCCCTTTACA GAGGGAAGAA GAGTCACATT 1980
TGACTGAGTA GAAAGTACTA AGGGCATCGT TCCAAAATTG GGGAGCCAAG TTTCCAACCT 2040
TTGTTCTTTT GAGAATGAGG GTGGGGATAT CACCCCACTC CCATCTTACC TCTCCCACTT 2100
AGCTGAGAGC TGAACCTAAC TGACCTAATT CCTGTGGTAG GTCATTTAAC ACCTGTGTTG 2160
AGGTGCTTGG GGATGGACAA GGAATTTCAG GGAAGAACCC GGGCACTTTG ACAGAGAATA 2220
AGACTGGTAG AGGGACCGCC AGTGCTGGGT TCCGGATGGA CTAAGGCTAC AGAAATGGAG 2280
CAGAGCTGGG CGCGGTGACT CACGCCTGAA ATTCCAGCAC TTTGGGAGGC TGAGGTGGGC 2340
AGATCACCTG AGGTCAGGAG TTCAAGACCA GCCTGGGCAA CATGGTGAAA CCCTGTCTCT 2400