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

TagContent
EnhancerAtlas ID
HS165-09979 
Organism
Homo sapiens 
Tissue/cell
Ramos 
Coordinate
chr3:47011840-47014650 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr3:47014265-47014286AAAAAAAAAAAGAAAGAAAGA-6.25
STAT1MA0137.3chr3:47012732-47012743TTTCCCAGAAA-6.02
STAT3MA0144.2chr3:47012732-47012743TTTCCCAGAAA-6.32
ZNF263MA0528.1chr3:47012652-47012673TCTCCCACTTCCCCATCCTCC-7.23
Number of super-enhancer constituents: 29             
IDCoordinateTissue/cell
SE_00943chr3:47011823-47013610Adrenal_Gland
SE_11155chr3:47006228-47021706CD20
SE_13638chr3:47012190-47014336CD34_Primary_RO01536
SE_16650chr3:47013004-47014113CD4_Naive_Primary_8pool
SE_18708chr3:47011981-47014192CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:47012241-47014117CD56
SE_22640chr3:47012989-47013833CD8_primiary
SE_23114chr3:47011818-47013099Colon_Crypt_1
SE_23114chr3:47013149-47013444Colon_Crypt_1
SE_23749chr3:47011867-47013045Colon_Crypt_2
SE_28630chr3:47011456-47013166Fetal_Intestine_Large
SE_31407chr3:47011864-47013611Gastric
SE_32585chr3:47012045-47013761GM12878
SE_40617chr3:47009514-47013782Left_Ventricle
SE_41619chr3:47011859-47013106LNCaP
SE_41619chr3:47013118-47013549LNCaP
SE_42118chr3:47006473-47013770Lung
SE_47478chr3:47011837-47013097Pancreas
SE_47478chr3:47013259-47013604Pancreas
SE_48306chr3:47011163-47013545Psoas_Muscle
SE_48684chr3:47011649-47013186Right_Atrium
SE_49453chr3:47011900-47013041Right_Ventricle
SE_50160chr3:47011783-47013586Sigmoid_Colon
SE_52388chr3:47011775-47013545Small_Intestine
SE_53507chr3:47011625-47012444Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr34701189147012451
chr34701328447013477
chr34701318947013256
Number: 1             
IDChromosomeStartEnd
GH03I046969chr34701142247014580
Enhancer Sequence
CTTCTTCCAT TGTGGCCCAG GGAAGCCAGA AGATTGGACA CCCCTGGATA ACAGGCATGA 60
GCCACTGTGC CTGGCCGGTA GCCACATTTC AAGGGCTTGA AAGTCACAGG TGGCCCATGG 120
CTACAGTACT AGACAGTGCA GATTAAAGAA CACTATCACT GCACAAAGTT CTAGTGAGCA 180
ACACTGCTGC TCTAATCTCT AGAGCCAGGT GACAACCAGG AATTGCTGGT TGCCTGGAAC 240
CTGCAACTTG ACAGCCAGAC CTCAGCCCCA AGGGCTGGTC AGCCAGACAG CCAGTCTCCC 300
TGTCTCAGAG CAGCAAGAGA CAGCCCAATT CAGGGCAATC GCTCAGGAAA GCTTGGCATG 360
TTTATGCCAA GTTAATCATC ACCTTTAGAG AGCCTCCATT TGGCTGCTGA AGAAGAAAGA 420
GGTCAAAGGA GGACAGAGTG GCCTCACACT GCCCTGCCGG ACAGCACTGT AAAGAGATGC 480
CAGAGTTTCA TCCACACAGC CTTGAACTGT TCACCTACTC ACCCAGCCAG GAACTTCTGG 540
ATGAGCATCA GGAAATGAGG TTCAAATACA ATACAGAAAA GTGTGCCCAG GCTGGCTACC 600
ATCCCTGCTG GAAACCCTGG CTCTTGCAAA ACTTGGCTAC CAGAGTACCC CAGTCCAGCA 660
CTTTCAGACT GTACCCCTGC CCCTGTATCA CTGCCAAGTG CTTGCTGTCA AACTCCCTGG 720
AGCATCTCCA CTCTCACCTC TATGCACCTG AATGTTCCCA CCTCTAAAAT GCTCCCTGGG 780
AACACTCTCC TTTCCAGCTA CCTCGATGAC CTTCTCCCAC TTCCCCATCC TCCGTGGCTC 840
AGCTCAAGTT CCATGCTGCC TTCCCATGAA GCTTCCTCAG GCTCTGCCTG GCTTTCCCAG 900
AAAATGAACC CCAGCAGTAC TGTCTTTCTG CGTGTCAACG GGAACTGGCT GACCTACAAG 960
ATGCTGCTTC AGGCAGTGCT GTGTCCTCTA CAGAATCCCC TTCCCCCAGG GGGTCTTGCA 1020
TGGGCTGGAA TCCTGGAATC CAGGAGACAT TACTTCCCCT CCTCAGCCTT GGACATCCCA 1080
GCTCTCCTCA GCCTCTTGCC TTGCTCCTCT CACTAATAAG TGGCATCAGG TGGGCTGACC 1140
AGGACGTCTT TGTAAAACTA CAGCTGCATG ACTACAAGAG AGTTTTGCGC AGAATAATAC 1200
ACGGAAACAT TGCAACCCCT AATCTTGTCT CTTTCCATCT GCCACAACCT CAGGACCCTG 1260
AATTGTCTTA ATATCACTAA ATTATGAGTT TATAGTCTGG TGAGAGTTAG GAAGAAAGAT 1320
AAAACTGTGA GGAAAACCAA CTCCATGCCT GAAATTCCTA AGGCCTCCAG CAAAACCATG 1380
CCCACAGTAA GAACTCAATG AAGGACCTGC CACTGAGTGC TAGGAAACCA GCAAGATGCC 1440
ATCCTCATGG GGCAGACAGG TGCTCTCCAA GTGCAGGCAG AGAAGGTGCT CAATCCTGGT 1500
GTCTGTTGTC ACATCAGAAA CCTGAACTAA AAATGTGAAG CCGCTTCCTC TCTGAAGGAG 1560
GAGACTCAAG GGGTTTTATC TGGCCACAGC AGGCAGTCAT ACTTCCTCAC CAGACTCCCC 1620
ACTTAAAAGG TCCAGCAGAA AGGGCCACAG GCTGGAAAAT CAACTCAAAG GTTAGACCCT 1680
TACCTGTCCT GTCCCCAGGC ATTCACCTTA ATAAAAAAAA TCACTCAAGA ACTATAGGGA 1740
TTAAATATGA CACTAAAAAT ACATGCAACA AAATCAAAAA CAGATAAATT GAACTTCATC 1800
AAATTTTAAA CTCTTTGCGC AGCAAATGAG ACTATCCACC AGGTGCGGTG GTTCACACCT 1860
GTAATCCCAA CACTTTGGGA GGCCAAAGCA GGAGGACTGC CTGAGGCCAG GTGTTTGAGA 1920
TCAGCTTGGG AAACACAGTG AGACCCCCAT CTCTACAAAA AATTAATTTT TAAAAAAATG 1980
ACACTACTAA GAGAATGAAA AGATAATCCA GAGAATGGGA AAAAATATCA CTAATCTCAT 2040
CTCTAATAAT GATTTAATAT CCAGAATATA TGAACAATTC AATGACAACT CAATAACAAG 2100
AAAAAGAGCC CAATTAAAAA TATGGGCAAA AGGAATCTGG ATACTTCTTC AAAGAAAATA 2160
TATATACAAG TGGCAAACAA GCATATGAAA GGATGTTCAA CATCACTCAT CACTGGGGAA 2220
ATGCAAATCA AAACCACAAT GGGATACCAC CACTTCACAC CCATTAGGAA GGTTATAATT 2280
AAAAAAACGA AAAAAGAAGA TGGCTGGGCT TGGTGGCTCA CACTTGTAAT CCTAGCATTT 2340
TTGGAGGCCA AGGCAGGAGG ATCACTTGAA CCCAGGAGTT CAAGACCGGC CTGGGGCAAC 2400
ACAGTGAGAC TCCTGACTCC TTTAAAAAAA AAAAAAGAAA GAAAGAAAAT AAAATAATAA 2460
GTGCTGGGGA GGATGTGGAG AAACTGGAAG CCTTGCACAC TGCTGCTGGG AATGTAAATG 2520
GTGCAGCCAC TACTGAAAAC ACTATGGTGT TTCCTCAAAA AGCTAAACAG AATTATCATA 2580
TGATCCAGCT GTTTTCCCTA CACATAATTA CATTCCTCTC CCTGCTATAT AAACCCCTGA 2640
TTTTAGTTCG TCGAAAAGAC AGATTTGAGA CTGATCTCCC TTCTCCTCAC CTGACATCAC 2700
CCGAATTTAA AAAAAAAAAA AAGGCCCAGT GTGGTGGCTC ACGCCTGTAA TCCCAGCACT 2760
TTGGGAGGCC GAGGTGGGTG GATCACCTGA GGTCAGGAGT TTGAGACCAG 2810