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

TagContent
EnhancerAtlas ID
HS136-11538 
Organism
Homo sapiens 
Tissue/cell
Monocyte 
Coordinate
chr2:218798030-218800550 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs4672862chr2218798645hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr2:218799888-218799909AAGGCAGGGTGAGGAGGGGGA+6.01
ZNF263MA0528.1chr2:218799065-218799086TAAGGAGGACAGGGAGGGAGG+6.74
ZNF263MA0528.1chr2:218799897-218799918TGAGGAGGGGGAGGAAGGAGT+6.88
ZNF263MA0528.1chr2:218799894-218799915GGGTGAGGAGGGGGAGGAAGG+7.77
ZNF410MA0752.1chr2:218798601-218798618GAACATTATGGGGTGGA-6.05
Number of super-enhancer constituents: 32             
IDCoordinateTissue/cell
SE_00005chr2:218749169-218810848Adipose_Nuclei
SE_00853chr2:218797442-218803745Adrenal_Gland
SE_01533chr2:218790723-218809422Aorta
SE_02835chr2:218797452-218802706Astrocytes
SE_02897chr2:218797496-218801561Bladder
SE_03410chr2:218798315-218799120Brain_Angular_Gyrus
SE_04023chr2:218796939-218803023Brain_Anterior_Caudate
SE_05119chr2:218797043-218800487Brain_Cingulate_Gyrus
SE_05795chr2:218790958-218814655Brain_Hippocampus_Middle
SE_07532chr2:218797113-218800617Brain_Hippocampus_Middle_150
SE_08301chr2:218797227-218800541Brain_Inferior_Temporal_Lobe
SE_25781chr2:218782377-218810766Duodenum_Smooth_Muscle
SE_26522chr2:218779494-218809405Esophagus
SE_30619chr2:218796759-218800484Fetal_Muscle
SE_31466chr2:218797375-218803314Gastric
SE_37423chr2:218797315-218803080HSMMtube
SE_40583chr2:218761671-218809601Left_Ventricle
SE_46178chr2:218797701-218803015Osteoblasts
SE_46622chr2:218797956-218798667Ovary
SE_46622chr2:218798713-218800960Ovary
SE_47481chr2:218797521-218798700Pancreas
SE_47481chr2:218798900-218799585Pancreas
SE_47481chr2:218799714-218800350Pancreas
SE_48107chr2:218791336-218809391Psoas_Muscle
SE_48552chr2:218791081-218809387Right_Atrium
SE_49441chr2:218797474-218803702Right_Ventricle
SE_50265chr2:218797048-218809390Sigmoid_Colon
SE_51152chr2:218791005-218809355Skeletal_Muscle
SE_52433chr2:218790973-218803772Small_Intestine
SE_53299chr2:218792085-218809367Spleen
SE_54481chr2:218753378-218811875Stomach_Smooth_Muscle
SE_65278chr2:218797162-218803589Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr2218798822218799459
chr2218799602218799844
Number: 1             
IDChromosomeStartEnd
GH02I217926chr2218791134218803703
Enhancer Sequence
GATAGAAGAC AAAGCTGGCA TCAGCTAAAG ACCCGGTGAC CCAGACACTG CAGCCCTGCA 60
TACACACAGC TCAAAACAGC CCAAGGCACA CACAGCGCAC ATGCCTGACC ACTGCCGGAC 120
CCAGATACAA AGTCACCCCC TGGTGCTTGG GCCCCACCCC AACCAGAGCC ACACAAACAG 180
AAACACATCA GCACCGCCAA CACATCCACT GGCAGGGACA CTCTGCATGG CCCCAAGCAC 240
AGCCAATTCC AGGAAGCCAG AAGGGGAAAG GAGCCCATAT GTACAGACTG GAACAGGGGG 300
AGCATGAGCC AGCAGAGATG GGGGGAACAA GAGCAGCCCA GGGCCCCTGA AGCACACCCA 360
GACCTCCCAG CTCCTTTCAA AGTGCCCACT GCAGCCTTGG CAAGCAGCAA ATTCTCCTCA 420
CACTTGCCTG TCCCATCTGA GCCCCACCCA TCCTTCTGGA AGAGCAGGTG AAAGGATAAG 480
GCACACGGGC AGAAGCTGGG TGGGAGGTGT CAGAAATGGA AGAGCAGGTG CACAAACAAT 540
AGGGTGGAGT AGATAGGAGG ATACGCAGCC TGAACATTAT GGGGTGGAAG CACAGGTAGC 600
TGGAATTTTA GGGACAGAGG TGGTGAGGAA GGGCAAAACA GAGTTTAGGG CTCGGGACAA 660
CCATATTATT TGAACACATA CAAAGAACAT GTACTTCATA CAGATTATCC CATTTAATCC 720
TTCCAACAAG AGATTCAACA AGCAGTAGCC TCTTTTCACA TATGAGGCTA CTGAACCTTA 780
CAGCGGAGAA ATGTGTTGGC CAAGGTCACA CAGCGATGAG TGGTTGAGCT GGGACTCAAA 840
CCCAGGACAG CCAGACTGCA AATTCTACAC TCCTTGAGGC AAGCCAAGTC ACCTGGATGC 900
TTGGAAGACA AGACAGAGCA TCGATGGAGC TGAGGGGGTG TGAAGGCATA GGTGATGGGA 960
GGGGCTGATC CAGAGAAGCA CAGAGAGGCA GAGGGGATGA GGTGTGGCAC CCTGCTGGCC 1020
GGGACCCCCA GCTCCTAAGG AGGACAGGGA GGGAGGAGCT CAGGCTGCTG TGATTCAGTG 1080
GCTGGGCCTC CGGGGAGAAT TTCCGGAGCC CCAGACAGCT CTGTGCAGTC TAGGAGCCAC 1140
CTACCCAGTG GAGACACTGA GCCATTACTC ACAACTGTTA CTCACTTTGC CTCTGCACCC 1200
CCATCCCCAG CACATCACTT CCTCCCACTC TGTTCCCTTT GGGTGGCCAA GGCAGGCAGC 1260
AGATCTTCCC CAGTCCCCTC CTTTGCTTCA TTGGCTCCAA TCCTGCCAAG CGTATCCCCA 1320
CCTGAGTCAC TGGGACAGAG ACGGGAGATT CTGGCCAGCC CAACCCTGAC AGCTGTTGCC 1380
CTCTGCTCTG TTCCAAGAAA TCAAGCTGCC TGGAGGAGTG GTCACTGGGC AAAGAACGTT 1440
CCAATTCCAG TGCTGGAAGG ACCTCCCCAG CATTTCAGAT GGCATCCCAG CAGATGCCTG 1500
AAGAGCCAAC AGGATCCCAC CTCGATGCTG GACAGCTCTG CCAAAGGCCC CAAGACTAGG 1560
AGCCTCTCTG TTCAGAAAGA TCCATGCACT TACAGAATTT CAGCACTGCT GAAAAGAGAG 1620
AACGCCCCTA ACTCGAACTT CTCATTTCGC AATTGAGGAA ACCAAAGCCC AAAAAGTGGA 1680
AGCAATTTGC CTGAAGTCAC ACAGTGCCAA AAGGGACTAG CAGGTCACCT GACGCCCCTG 1740
CCACAGGTCC TTCCGCGGCA CTACACAGAC CTCTCTCTCT GCCCCAAGTC AGAGCAGGCC 1800
CCTGAAGTTG ACTCTGTCAC CCTCCTGTTG CAAAGCAGTG CTGAAGACGG GAGATCTGAA 1860
GGCAGGGTGA GGAGGGGGAG GAAGGAGTTG CAGCCAGACA GCGGTTACTG GGGAGGAATC 1920
ACTTTCCAAC AGTGAAGGGG CACTGGACTC CAGGCCACCT ACTCAGAACA GTCTGCCCAG 1980
GAGGCAGGGA GATGGACTGC AGGCCCTCCG GAGGCTCTGG AGCTCAAGGG CCAGGCCCTC 2040
TGGCAGGAGA TGATGGGAGG AATTCTTAGG GTCCCAGCTG GGAACTTGGG AGAGTCATGG 2100
CCTCCTCTCC AATCACCTCT CCTCCCCCAG CCCCCACCCC TCACCCTGGC TCGCCTCTGC 2160
TCTCCCAGGG CTCCAGCCTG GAATCCAGAC CTGACCACTG CCTCCACTCC CACGCTTGGC 2220
CTAGCTCAGC CGGCCACAGC AGAGGCAGCC ACATGTGTGG TGGTGGAAGC AGTTCGTGAG 2280
CCACCGAATT CCTTCTAAGC CTCCAGAGGA GCCTCATCTA TCTCTTGTGC TCTCCCCTCC 2340
CACTCTGGGC AGTTGCACTC ATCCCAGCCA AGAAACCCCT GCTGCCAGCC CCACTCTCTC 2400
CCACTGTATC AATAATAGTA ATAACCATAA CAAAAACAGC AATAACAATC ACCAAGGTTT 2460
ATGCAGAACA GCCTGCATGC CAGACCCGCT CTATTTGTTT CCTGCATTTT ACAGGTGAGC 2520