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

TagContent
EnhancerAtlas ID
HS060-24223 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr3:47000530-47002910 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs7628747chr347001990hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
KLF4MA0039.3chr3:47002493-47002504GGAGGGTGTGG-6.32
RREB1MA0073.1chr3:47002555-47002575TGTGTGGTGGTGTTGTGAGG-6.32
Sox6MA0515.1chr3:47001954-47001964AAAACAATGG-6.02
Number of super-enhancer constituents: 38             
IDCoordinateTissue/cell
SE_00943chr3:47000636-47003247Adrenal_Gland
SE_02008chr3:47000692-47002741Aorta
SE_11155chr3:46999721-47003820CD20
SE_14564chr3:47000278-47001837CD4_Memory_Primary_7pool
SE_16650chr3:46999983-47001584CD4_Naive_Primary_8pool
SE_18708chr3:46999601-47003619CD4p_CD25-_Il17-_PMAstim_Th
SE_20061chr3:46999416-47002518CD56
SE_20061chr3:47002557-47003528CD56
SE_22640chr3:46999598-47002488CD8_primiary
SE_22640chr3:47002498-47003619CD8_primiary
SE_23114chr3:47000575-47002747Colon_Crypt_1
SE_23749chr3:47000733-47001255Colon_Crypt_2
SE_23749chr3:47001324-47001875Colon_Crypt_2
SE_23749chr3:47002233-47002725Colon_Crypt_2
SE_26114chr3:46999989-47002735Duodenum_Smooth_Muscle
SE_28630chr3:46998170-47003223Fetal_Intestine_Large
SE_30558chr3:47000885-47002668Fetal_Muscle
SE_31407chr3:47000683-47003179Gastric
SE_32585chr3:47000613-47001820GM12878
SE_38780chr3:47000232-47003616HUVEC
SE_40617chr3:46999813-47003535Left_Ventricle
SE_41619chr3:47000640-47002043LNCaP
SE_41619chr3:47002075-47002794LNCaP
SE_42118chr3:46999822-47003340Lung
SE_47478chr3:47000658-47001925Pancreas
SE_47478chr3:47001962-47002754Pancreas
SE_48306chr3:46999915-47003370Psoas_Muscle
SE_48684chr3:47000717-47002767Right_Atrium
SE_49453chr3:47000756-47002110Right_Ventricle
SE_49453chr3:47002144-47002748Right_Ventricle
SE_50160chr3:46999961-47003286Sigmoid_Colon
SE_52388chr3:46999875-47002632Small_Intestine
SE_53507chr3:47000017-47003202Spleen
SE_58746chr3:46966845-47032612Ly1
SE_59747chr3:46966600-47033537Ly4
SE_60850chr3:46965041-47030117DHL6
SE_62445chr3:46966331-47033109Tonsil
SE_64772chr3:47001706-47002732NHEK
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr34700132347001648
chr34700166647002342
chr34700078147001063
chr34700066747001400
Number: 1             
IDChromosomeStartEnd
GH03I046952chr34699369247003318
Enhancer Sequence
CTGAGAAGTA AAGGTAAGAC AGCTGTCTGC TCTCTGGTGT GATCTACAAG TGATAAAAAT 60
CCTAATTAAA CCAAATTTAA ACAAGTCAGA ACTGGCACAT TTTTTTGTGG GGGGAAATAC 120
TGCTTCACAA GGTCTTATCC CCACCTACAC ACACTTCCTT TAGCTACAAA GCGTTTTTAA 180
AAATCCACAT GCTCAGCATA TGGAAAGGTT GAGAAAGCAG AACCACATGA GGAGTCAATA 240
CCCAGCACTA ACAACTGTGT ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA 300
GTTTCTTCAA CTGCTAGATG GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC 360
TGTGGCTGGC ACAGAGTACG TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT 420
GGAGCCTGAG ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG 480
GTCACATAAC AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC 540
CATCAGTGTC ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA 600
GCAGACCCTA CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG 660
GGGGACAGGG AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC 720
CACCTCCATG CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT 780
TTCACACCTG GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC 840
TCAGCACCTC TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA 900
AATGGGGACA CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT 960
GGGTTGAGCG CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA 1020
TGCCCTCCCT CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA 1080
CAGTATTATA CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC 1140
TTGAGGCAAG GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG 1200
CCTCAACAAT AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG 1260
CCCAGCATTC ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG 1320
CCCAGGACAG GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA 1380
GGATTCAAAT TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG 1440
GGCTGTCCTT GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA 1500
GCAGCTCTTT AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG 1560
CACCGTTGCC GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC 1620
TTCCCTCCAA AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA 1680
AGGAAGGAAG AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA 1740
TCTCCGAACA ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA 1800
GGGAAAGGCA AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG 1860
GTGTGTATGA GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC 1920
ATGTGGAGGG GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA 1980
GGGAGGTACT ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG 2040
TGAGGTTAAG GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA 2100
GTACATGCTG TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG 2160
GTTACAGAAA ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA 2220
TTGCATTTCA TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG 2280
TCTGCAGGGT CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA 2340
ACTGACCCTG AAGCAACTAT CGGAGGTAAC ACATATTTCT 2380