EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS030-11332 
Organism
Homo sapiens 
Tissue/cell
CyT49 
Coordinate
chr3:42066110-42068390 
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr3:42067595-42067613CCCTCCATCCCTCCTTTC-6.17
HES2MA0616.2chr3:42068158-42068168GGCACGTGCC+6.02
HES2MA0616.2chr3:42068158-42068168GGCACGTGCC-6.02
MyogMA0500.1chr3:42067968-42067979CTGCAGCTGTT-6.02
Tcf12MA0521.1chr3:42067968-42067979CTGCAGCTGTT-6.62
ZNF263MA0528.1chr3:42067591-42067612CTCTCCCTCCATCCCTCCTTT-6.38
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00063chr3:42060660-42068971Adipose_Nuclei
SE_01171chr3:42066131-42066552Adrenal_Gland
SE_01171chr3:42066556-42067516Adrenal_Gland
SE_01171chr3:42067617-42068091Adrenal_Gland
SE_01796chr3:42066168-42066949Aorta
SE_02512chr3:42065459-42068129Astrocytes
SE_10226chr3:42065877-42068137CD19_Primary
SE_10922chr3:42060609-42068638CD20
SE_23272chr3:42066116-42066919Colon_Crypt_1
SE_23272chr3:42066976-42067316Colon_Crypt_1
SE_24262chr3:42066235-42066832Colon_Crypt_2
SE_24991chr3:42066143-42066941Colon_Crypt_3
SE_24991chr3:42067525-42067991Colon_Crypt_3
SE_25861chr3:42065366-42068715Duodenum_Smooth_Muscle
SE_26989chr3:42066043-42067298Esophagus
SE_29565chr3:42065389-42069132Fetal_Muscle
SE_36966chr3:42065344-42069055HSMMtube
SE_38230chr3:42065373-42068528HUVEC
SE_40683chr3:42066021-42068361Left_Ventricle
SE_42248chr3:42066070-42068146Lung
SE_44658chr3:42065460-42068844NHDF-Ad
SE_44918chr3:42065870-42068385NHLF
SE_45733chr3:42065416-42068758Osteoblasts
SE_48185chr3:42066028-42068146Psoas_Muscle
SE_48670chr3:42066166-42067443Right_Atrium
SE_48670chr3:42067563-42068128Right_Atrium
SE_49555chr3:42066577-42066889Right_Ventricle
SE_50309chr3:42066089-42067441Sigmoid_Colon
SE_51166chr3:42060817-42068845Skeletal_Muscle
SE_51885chr3:42065989-42068136Skeletal_Muscle_Myoblast
SE_52625chr3:42066102-42067523Small_Intestine
SE_52625chr3:42067553-42068124Small_Intestine
SE_53513chr3:42066102-42068146Spleen
SE_54717chr3:42065389-42068637Stomach_Smooth_Muscle
SE_62800chr3:42053253-42125059Tonsil
SE_63663chr3:42065927-42068150HSMM
SE_65769chr3:42066166-42068375Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr34206711042067525
Number: 1             
IDChromosomeStartEnd
GH03I042019chr34206049442069114
Enhancer Sequence
CAGTAGATGA AGTTAATGAT TGCCCACTTT CAGCTAATCA TATGATTGCT ATTGAAATAA 60
GTACTTGCTA GACAGGGATA GAATCTAGTA ATTTGTTAGC TTCAGTACTT CATGCTTGCA 120
TACACACCCA TGCTATTGTG TTACCAAGCC TGAGTTTTGA AATGTGGCGT TCTTTGTCTT 180
TTTCTGGTGA ATAAACCCCA TACGTCTTAC CATAGCCATT TGACTCTTCC TGGCTGTCAG 240
GATGTGTTGC CCTGGACTGA GAGTGAGAGA TCCCAGATTT TTCAGCTTCT CTTCCAATTG 300
CTAGGGATAC CACATCAGTG CCAACGTGAG TCTCCTCTTG TCACTTTCTG CTAGGCTTCC 360
CCTTAGAAGC TGAAATTCTT TCCCTTCCTG ATGCTAAGTT GCAGTTTCTT AAAATGCTAG 420
AGAGCTTTTA AAAGCATACC GTGATGGGAA TTAGTTTCAA AAGATTATAC CAGAGGGGGT 480
TAAAACTTGC CAACCTTGTA AAAACCTAAC TTCTTTGTTT ACGTCCTCCC TGCCCCGCTT 540
TCTGCTGTGC TTGGTTTCCT CCTAGCAATA TGCCTTGGTC AGGGGGAGAG TCTTCCTGTC 600
AGACATAACT TCCCAGACCA GCACTCCTGG AGGGGCCTGT ACCTCAGACC CTGGCAACGA 660
GGCACGCTGG GGCACGCTGG CCTTTCGTTG TGGTGTAGAA AATTTTTCAT TTGGAATTCC 720
ATTTTAAAAA TAAGTATAGG GTTATTTATA TCTTCTTACA TTAATTTTGA TAAGTTGTGT 780
ATTTTAAGGG CTTTATCCAC TTTATCTAAG CTACTGAATT AATTGGCACA ATTATTACTC 840
TTTCAATGTC CATAAGACCT GTAGTGATGT CCCCATATTT TATTTCTGGT ATTTGCCTTT 900
CATGTTAAGA ATGTGTCTGT TCAAAGGGAG AGGGGAAGGA GAAAAGAAGA ATGTGTCTGT 960
TCAAAGGACT GCTGGATCAG GGTAACTTAG CTCAAGAAAA TGAGAAGGGG TGGTTTCTGG 1020
AAGGGGAGAA TGAAAGCCGT GGAGGAAATA AAGCATGAAT GTGGGGGAGG GCGGGGGCGG 1080
GGACTGCTTC TCTTGCTGGC TGCCTTCTCT CTCTGGAGAA TCTGCTGGAG AAGGAGCAGT 1140
CACGTGGGTG GTGAGCTCAT TAGGCTGGGG ACACCAGCTG TGCTATTATT AGGGCTTTTA 1200
AAGTCCGTGG CAGATGTTCT TAGGCGGTGT TCCAGCCTTG TTCACTTCCC ACATATGGCA 1260
TGATACTGTA CACAGAAAAA AGAGGGACTC TTTAACAAAT AGCTTTTCCA TGAAATGCAT 1320
CACTATTTTT TTCCCATGAA CTTTTTTCTT TTCTTTCTTC CTCTGTCTCT GTTTCTTTGT 1380
TTCTCTCTCT GCTGTTTGTT CTTTCTTCTT TCTCCGTTTA TCTTTCTCCC TCTGTCTCTT 1440
TCTTGCTTTC CTCTATTTTT CTGTATTCTC ATTCTCCCTG TCTCTCCCTC CATCCCTCCT 1500
TTCTATACTT CCTTCTTTTG TCCTTTGAGG CCCTTTTTAT TTAATCCTTT GTGAAACTAG 1560
AAGAGGACTC AGAGGCACAT GAAGAAAGTT TGTCTATTTT AGATTAAAAG TGAGCCTTAG 1620
CATTTCATAG AAAGTATAAG AAATGTGGGT AAGTCTCAGG GTGATCATAT ACTAGAGAAT 1680
TTTTTTGACA AGAGCCTGTT TTGAATTGCG TGGTTAGCTT GCTGCCTCTT CACTCCTCTG 1740
GCACAGTGGT AGTTTTTGTA CAGGATCGCT TTTACCTCAA TGGACTGATA AGCTAGCCAG 1800
GGCACCGATT ATTTTTACAT ACCAATTTGT GTGTTGTTTG TTTGGCTAAT CACCTCTTCT 1860
GCAGCTGTTA TCCTGGATCT CAGTGATCAA AGAGATCAGT GATCTCTTTT TTTTTTTTTT 1920
TTTTGAGACA GAGTCTCACT CTGTTGCCCA GGCTAGAGTG CAGTGGCATG ATCTCAGCTC 1980
ACTGCAACCT CTGCCTCCCA GGTTCAAGTG ATTCTCCTGC CTCAGCCTCC CGAGTAGCTG 2040
AGACTACAGG CACGTGCCAC CACGCCTGGC TAATTTTTGT ATTTTTAGTA GAGATGGAAT 2100
TTCACCATGT TGGCCAGGCT GGTCTTGAAC TCCCGACCTC AGGTGATCTG CCTGCCTCGG 2160
CCTCCCAAAG TGCTGGGATT ACAGGCGTGA GCCACTGCGC CTGGCCAGTG ATCAACTTTT 2220
GTCAGTAAGC TTCCATGTGT AGACCCTCCT TCTCCCCTCA TATTTATAGT AACCCATGTC 2280