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

TagContent
EnhancerAtlas ID
HS076-39703 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr3:46979000-46981090 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF2MA0051.1chr3:46980451-46980469CTTCTGCTTTCGCTTTCT-6.03
OLIG2MA0678.1chr3:46980762-46980772ACCATATGGT+6.02
OLIG2MA0678.1chr3:46980762-46980772ACCATATGGT-6.02
ZNF263MA0528.1chr3:46980841-46980862CGAGGAGGGGGAGGGGTGGGG+6.09
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00943chr3:46975428-46979987Adrenal_Gland
SE_00943chr3:46980333-46981726Adrenal_Gland
SE_02008chr3:46975431-46979976Aorta
SE_10127chr3:46964000-46982704CD14
SE_11155chr3:46963907-46992913CD20
SE_13638chr3:46980712-46981666CD34_Primary_RO01536
SE_14564chr3:46978732-46979799CD4_Memory_Primary_7pool
SE_18708chr3:46980160-46982000CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46978908-46982117CD56
SE_22640chr3:46980363-46981782CD8_primiary
SE_23114chr3:46980748-46981882Colon_Crypt_1
SE_23749chr3:46980358-46980679Colon_Crypt_2
SE_26114chr3:46979133-46981524Duodenum_Smooth_Muscle
SE_27403chr3:46970664-46979932Esophagus
SE_28630chr3:46978954-46982854Fetal_Intestine_Large
SE_31407chr3:46975429-46987226Gastric
SE_32585chr3:46980183-46981538GM12878
SE_38780chr3:46975376-46979404HUVEC
SE_40617chr3:46975387-46993135Left_Ventricle
SE_42118chr3:46970032-46992962Lung
SE_47478chr3:46979272-46979846Pancreas
SE_47478chr3:46980441-46980925Pancreas
SE_48306chr3:46975337-46979878Psoas_Muscle
SE_48306chr3:46980232-46981880Psoas_Muscle
SE_48684chr3:46975375-46980001Right_Atrium
SE_48684chr3:46980144-46982584Right_Atrium
SE_49453chr3:46977342-46979943Right_Ventricle
SE_49453chr3:46980881-46982106Right_Ventricle
SE_52388chr3:46980031-46981883Small_Intestine
SE_53507chr3:46980105-46981851Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59412chr3:46966960-46998383Ly3
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_65471chr3:46977753-46993036Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34698033846980600
Number: 1             
IDChromosomeStartEnd
GH03I046924chr34696632946982223
Enhancer Sequence
ATGCTCACTG GCGAATGGCC TCAGGGGTCA TCTCTCCAAT GGACTGGAAG GTCACTTCTT 60
TCTCTCCAGT GGCAAAGGAG GCTGTAGCAG GGGCTATGGC CTAGGGGGTT CTCTGGAATC 120
AGCTCCCAAT CCATAAGCAT CCTGCATGAG AGCCCCTTTC CAGACTTGGG GTACAAATAA 180
AAAGCAAGAT CCCCTGGGAT GGACACGGCC TCTGCTGCAT CCTGCTCTTC CTGGAAAGTC 240
CATCATCCCC AATCCCTGGA CCCTGCAGTC TAAAGTTACG TCCACATAGG TCTGGCCCTG 300
TGTTAGGCAA CCAATGTTCT AATCTGCCTT CCTAAATAAC CTGAGCAAGC CCTCTGCTCT 360
GGATCTGTTA AAGTCAGAAG AGTCTGCTTT TCTCTGGGGC CTACAAATAC AGGCACAACT 420
CCTTGCTAAG GCTAGGCTTC CTGGCAACCA AGGGAGTGAC CGAGTAGCAG GCCCTGCCAG 480
GTACAGGATG CTAGAAGTCC ACCTGCCCAA AGTCTCTAGA AGGACAGCCC CAAAAGCCAA 540
GCTCTCAACG ACTGGGAGGC AAACCTGTTC CACCATGCTC CACTGCCTCA AAAGAGGCCA 600
GATTAGAGCA AAGCAGAAGA ATATGATGAG CTGAAGCAGA ACCCAATTCA ATGTCCAGCA 660
TGGTTGGTCC CTGGGCTGCG GTGAGAAAAA ACAAAACAGG GCCCTGCACC TGCCCAGCTC 720
AGTGGGCTCA GGACAGGGCC TCAGAGCAGG TCTTGTGCTC CACTACAAAT GACCTGTAAG 780
ACCTAACAGG AAGCAGGTCC TCACATGGCA GGGCCTCTTT TATCTAGAAC TCACTGACAG 840
GAGCCTGGAA CTACACATGC CCTTTGGTTT TTTTCCCACA GTTTTCATTA TGATATATCT 900
CAGGCACACA GAAAAGTCCG GAGAATAACC TAACACATAT ACTCACCTCC TGCAGAGTCA 960
ATAAAAGTAA TGTTTTGCCA TATTCCAGAC AGGTTTGTTC CCCTCCTGTT TTTTTTTTTT 1020
TTTTTTTTTT TTTGGTACAA CAAAATCACA CATCATTGGC CAGGTCCACT GGCTCACACC 1080
TGTAATTCCA ACACTTTTGG GAGGCTGAAG TGGGTGGACT GCCTGAGCTC AGGAGTTTGA 1140
GACCAGCCTG GGCAACCTGG TGAAACCATG TTGTTTTTGT ACCAAAAATT AGCTGGGCAT 1200
AGTGGTGCGC ACCTGTGGTC CCAGCTTCTT GGGAGGCTGA GGTGGGAAGA TCGCTTGAGC 1260
TTGGGAGCCA CGTGGAGGTT GCAGTGAACT GAGATAGCGC CACTGCACTC CAGCCTGGGT 1320
GACAGAGCGA GACCCCATCT CAAAAAAAAG AAAAAAAAAA TCACACATCA TAGAGCCTTT 1380
CCCTAATCCT GTTTCCTCCT TGCTTCCCCA GACAGCAATC GGAGGCATCA CTCCTCATGT 1440
ATGTGTTTAC ACTTCTGCTT TCGCTTTCTT GGCAGCACCT GACACTGTAT CACACGCCTG 1500
CTTCTTCGTT AACAGCCTGT CTCCTTCCAG AAAATGTCAG CTCCATGAGG GTAGGGGCTG 1560
TACTTTGTCT GCTGTTGCCT TCCAGGGGCC CACAATGGTG CCCTGCACAG AGCAGACAAC 1620
CAATAAAGTC AGTACTTGCC AACTGAGTAA CACACATATA TCATTTTGTG TTCCTAAATT 1680
TGATATAAAT GTTCCTGCCC TGTATGCCTC AATTCTGAAA CCTGCTTTTT TCCTTCACTC 1740
AACACCATGT TTGAGATTCA CAACCATATG GTTCAACATT CAAGCCTCTT ACTGTATGAC 1800
CCACCCACCC ACCTGCTAAA CCAGCGACCC TTCTCTCTCA TCGAGGAGGG GGAGGGGTGG 1860
GGATCAGAGA AAACACCACC AGCAAATCAA AGCCCAGAAA CTGGAACTCA GGCTCCAGCC 1920
AGAGTTCCAG TTTTTGAGAA ACTAAGAATA AACCAGAAGA CCAAAGGGCC TCTAATATGT 1980
AGTTACCACA GAATGGGGGA AACTGTGCCA GCACCCACCC ATAAAGCCAC ATATGTTGGG 2040
GTCACCTGGC AAAGGAGCAA CTAACTGGCC TTCATCTTCC CATCACCAGC 2090