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

TagContent
EnhancerAtlas ID
HS191-25806 
Organism
Homo sapiens 
Tissue/cell
Trophoblast 
Coordinate
chr3:47000720-47003300 
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: 39             
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_47478chr3:47002902-47003205Pancreas
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: 3             
ChromosomeStartEnd
chr34700132347001648
chr34700166647002342
chr34700078147001063
Number: 1             
IDChromosomeStartEnd
GH03I046952chr34699369247003318
Enhancer Sequence
GCTCAGCATA TGGAAAGGTT GAGAAAGCAG AACCACATGA GGAGTCAATA CCCAGCACTA 60
ACAACTGTGT ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA GTTTCTTCAA 120
CTGCTAGATG GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC TGTGGCTGGC 180
ACAGAGTACG TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT GGAGCCTGAG 240
ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC 300
AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC 360
ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA 420
CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG 480
AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG 540
CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG 600
GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC 660
TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA 720
CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG 780
CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT 840
CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA 900
CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG 960
GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT 1020
AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC 1080
ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG 1140
GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT 1200
TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT 1260
GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT 1320
AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC 1380
GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA 1440
AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG 1500
AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA 1560
ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA 1620
AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA 1680
GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG 1740
GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT 1800
ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG 1860
GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG 1920
TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG GTTACAGAAA 1980
ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA TTGCATTTCA 2040
TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG TCTGCAGGGT 2100
CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA ACTGACCCTG 2160
AAGCAACTAT CGGAGGTAAC ACATATTTCT AGTCAGAACA CCCCTGGCTC GGTAGGTCCA 2220
GAGTATGGAC AGAGTCTGGC TAGCAGGTCA GGAGGCCAGC ACTGGAGGGC CTGGCTCAGC 2280
AGGTCCTTGT CTTCCCTGGG AGTCCATGTT GTCTTTTCTC TAGTGCACAA AGCCTAAGGG 2340
GCTCAGAGTC ACAGGACGCA GCATACCCAC TACAGTGCCA TGGGGCACCC AGGAAATGTC 2400
TGAATGTTTT GTTAAAATAA GTTTAAGAGT TGTCTCTGCC TACAAGGAAC TGCCTGTCCA 2460
CTGAAGGGGT GGCATGAATT GGGACTTAGA AGCATGAAAA AACAAATATA TTTTAGCAGC 2520
TACCACTGCT ACTACTACTA CTACTATATG TACAATGACA ATTATCAGGA TGTTATGGAA 2580