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

TagContent
EnhancerAtlas ID
HS116-20337 
Organism
Homo sapiens 
Tissue/cell
Left_ventricle 
Coordinate
chr2:238614720-238617030 
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Nr2f6(var.2)MA0728.1chr2:238615489-238615504CGAACTCTTGACCTC-6.24
ZNF263MA0528.1chr2:238615228-238615249TCCTTCTCTGTCTCCTCCCTC-6.11
ZNF263MA0528.1chr2:238615225-238615246CTTTCCTTCTCTGTCTCCTCC-6.58
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00318chr2:238614544-238615875Adipose_Nuclei
SE_00318chr2:238615894-238617293Adipose_Nuclei
SE_01566chr2:238612977-238617649Aorta
SE_09199chr2:238608075-238617357CD14
SE_11030chr2:238614296-238617234CD20
SE_13435chr2:238614109-238614995CD34_Primary_RO01536
SE_13435chr2:238615919-238617077CD34_Primary_RO01536
SE_17380chr2:238614307-238617265CD4p_CD25-_CD45RAp_Naive
SE_17823chr2:238594491-238617199CD4p_CD25-_CD45ROp_Memory
SE_18373chr2:238615404-238617031CD4p_CD25-_Il17-_PMAstim_Th
SE_19179chr2:238608152-238616656CD4p_CD25-_Il17p_PMAstim_Th17
SE_20077chr2:238615517-238617022CD56
SE_22424chr2:238615547-238617103CD8_primiary
SE_23963chr2:238615026-238615313Colon_Crypt_2
SE_23963chr2:238616491-238616771Colon_Crypt_2
SE_25815chr2:238608299-238618181Duodenum_Smooth_Muscle
SE_26722chr2:238615339-238617681Esophagus
SE_29463chr2:238612762-238614953Fetal_Intestine_Large
SE_29646chr2:238615478-238617730Fetal_Muscle
SE_31908chr2:238616418-238616969Gastric
SE_36919chr2:238608262-238615293HSMMtube
SE_36919chr2:238615618-238618768HSMMtube
SE_40633chr2:238614535-238615385Left_Ventricle
SE_40633chr2:238615596-238618258Left_Ventricle
SE_42111chr2:238608226-238618523Lung
SE_44921chr2:238616101-238617119NHLF
SE_48071chr2:238614369-238617012Psoas_Muscle
SE_48757chr2:238616077-238617840Right_Atrium
SE_51094chr2:238608086-238615331Skeletal_Muscle
SE_51094chr2:238615393-238618500Skeletal_Muscle
SE_52590chr2:238615601-238616912Small_Intestine
SE_53427chr2:238615938-238616918Spleen
SE_54582chr2:238614727-238618024Stomach_Smooth_Muscle
SE_55444chr2:238615832-238616105Thymus
SE_55444chr2:238616192-238616904Thymus
SE_58523chr2:238563966-238621920Ly1
SE_59868chr2:238570692-238624050Ly4
SE_65656chr2:238614594-238615419Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2238616188238616491
chr2238615980238616918
Number: 2             
IDChromosomeStartEnd
GH02I237706chr2238615027238615313
GH02I237707chr2238615684238616735
Enhancer Sequence
GTGTCATCCA TTATGTCCAT GGTCCCACGC ACTCAGTGGG AGAGGGGTAT GCAGGGCAGG 60
TACACTAGTG GTGGGAGTCT TGGGGACCAA CCCAGAATTC CACGTTCCCA CACAGTGGGA 120
GAGGGGTATG CAGGGCGTGT ACACCAGAGT CTTGGGGACC AACCCAGAAT TTGGCCGACT 180
GCAGTTGTCT CTCCCTCTGT TCCCTTCTGG TGGCCCTTCT TTCCCCCAAC CCTTTCCTCT 240
TTCTTACATC TCACCCCTCT GCTCCTCTTC TTCTTCTTGC ATGGCCTCCC TTCTCTTTTC 300
CCGGCCCCTC CTCTCTGTTC CTCTGCCCCC CAACCCCCAA GCTGGTGGGC TATGGCTGCT 360
ATGAAACCTC GTACCTGCTC TGTACTGGCT TAGAAACTGA GCCAATGGCA CAGAGCCACC 420
TGCCTTACCA GGAAGGGCTG CACTTGGCGT GGCCTTGGTC ACTTTGCTGG CCCATTGGTA 480
GGGCCGTAGG ACGTCACTCT AATGCCTTTC CTTCTCTGTC TCCTCCCTCT TTGCTTTTGT 540
GTAGACCCAA GAGTCCTTTC TTTTGTTTGA GACAGGGTCT CACTCTGTCA CCCAGGCTGG 600
AGTGCAGTGG CACAATCACA GCTCACTACA GCCTCAACTT CCCAGGCTCC AGTGATCCTC 660
CCACCTCAGC CTCCCAAGTA GCTGGGACCA CAGGTGTGTG CTACCACACC TGGCTAGTTT 720
TTGTATTGTT GGTAGACACA GGGTTTTACC ATGTTACCCA GGCTGGTCTC GAACTCTTGA 780
CCTCAAGAGA TCCTACCTGC CACCGCCTTC CAAAGTGCTG GGATTCCAGG CCTGAGCCAC 840
CATGCCTAGC CTGGCCCCAA GAGGCCCTTC ACACCATGTA ATATGGTCTT GGAAATTGAA 900
AATGGCAACA AGGTATCAAA ATCCTGATGC AGTTGTGATT TTTGACACCC CTTGATTTGA 960
AAGACATGGG GTGGGTTGAT AAAGGAGCCA AGCGAATAGA ACAAATTCCT CATGAGGACA 1020
CAACCAGGCA ACCTCAAGAC GACAGATCAA GTGTGGCCAG TTTGCAACTT AGATTAAAAC 1080
TGAGAAAGAA GGTACATTTG TAATATAGTG TAAGTCTAGG ATGGGAGAGA GGGACGTCCC 1140
TGTCAGGACC ACCCCCATGC CAGGAGCTTG CTGGCCACCT CGGAAGTCCC ATTTTAATAT 1200
TATCTAGGAG CCGGTTGTGG TGGTGCAAAC CTGTAGTCCC AGCTACTCAG GAGGCTGAGG 1260
CAGGAGGGTT GCTAGAGCTC AGGAGTTCCT GGCTGCAGTG AGCTGTGATC ACACCTGTGA 1320
ATACACACAC ACACTGCACT TCAGCCTGGG CAACAGAACA AGACCTCATC CCCAAAGGAA 1380
AAAGAAAAAA AAAAAAAAGG AAGAAAAAAA GGAAAAGATT ATGTAAGACG TCTGAAAACT 1440
GTTTATAGAA CCATTGTTGG AAGGATTACA GACGTATTCT CAAAAAACAC TTCAGTAGAA 1500
AGAGGGTGGG GTTTGTTTGA TACCAGAAAA CCTGCACTCA GTAACACTTA TGCCATCGAG 1560
CTTACGGGGC TGTGGTATCA CATGAAGCAG TGAATACGCA TGCAGTTTTT AAAATGACTT 1620
GTAAGTTGTT TGTAGAAACA GTTCAGATGC CAGGCTCGAT AGCATCATGT CCATTCCTGC 1680
TCAAGCATTT GAAACGTTCT CACGGAGCAG AATGTGGCAG AACAGCTACA AGCTGAAAAA 1740
TACTTATATG GAGGCTGATT TTTTTAGTGC AAGGAAGGAC TCCAACAGCT AGAACCGTTC 1800
TGCTATGATC TTCATTGTGT TGGGAAAAGG TGGACTCCCA GCACGGCTGT GTTTTAAGGG 1860
GAAGCTGAGG GTGCGTGTGT GCTGAGAAGT GACTGGACAG CAGTTCGCTG GGATTACAGT 1920
CCCAGCTCCA CGCCAGCCAG CCCTATGGCC TCAGATGGGT CTGGCAGCCT CTCCAGGCCT 1980
TCACTTTCTG CTCTGTAAAG CGAGGGGTTG AACTGGAAAC CTGGAGTAGC ATCCAGCTGT 2040
TAACACTCTG CTCCATGCAT CTGTCAGAGC TCCAGAAGGA GGCTGACTGC CCAGCCCTGC 2100
CACCTACAGG CTGTGTGACC TTAGGCAAGT TACTTACCCT CTCTGTGCCT TCGTTCCCTC 2160
ATATTTAAAC TGGGGATGGT AACAGTCTCG GCCTAATGAG GCTGTTGCAA GGAATACATG 2220
GCATCATATC CATAAAGCTC TTAGAATATT CCTGCCTAGC ATGTGGTAAG GACTTGATAA 2280
ATGGTAGCAG TTCTTATAAC TATTTCTATT 2310