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

TagContent
EnhancerAtlas ID
HS095-20492 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr3:47000790-47002690 
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: 37             
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_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: 2             
ChromosomeStartEnd
chr34700132347001648
chr34700166647002342
Number: 1             
IDChromosomeStartEnd
GH03I046952chr34699369247003318
Enhancer Sequence
ACTGTGGTAC TCTGGGCCAG TTTAGCTTCT CAGAGCTGCA GTTTCTTCAA CTGCTAGATG 60
GCATGACTTA AGGGTACGCA TGTGAGTGAC AGCCCTACAC TGTGGCTGGC ACAGAGTACG 120
TCCTCAGTCA GTAGGCGCCA ACCACAGTGA TGATGATGGT GGAGCCTGAG ACTCTCACCT 180
GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC AGATCCCCAC 240
ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC ACCCGGAGGA 300
AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA CACGTGTGCA 360
GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG AGGTGGCAAG 420
GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG CCTGCCTGTT 480
CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG GAAACAGCTA 540
TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC TACCAGCTCA 600
GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA CTACTCATAA 660
GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG CTCTCCTCCA 720
CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT CCAAGACACT 780
GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA CCTGGGGGTA 840
CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG GGCCAGCCTC 900
ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT AACACTTGTA 960
ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC ACTCTCACTT 1020
CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG GAAAGTCCTG 1080
CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT TACCCTGCAA 1140
GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT GAAAGGACAA 1200
ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT AGAGCCCTGA 1260
ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC GAAGCAACTG 1320
TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA AACAAAACCA 1380
GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG AGGGCCAGGC 1440
ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA ACTGGCTTAG 1500
AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA AATTGTGGGT 1560
ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA GATATGTATT 1620
GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG GTGCTGTGGA 1680
GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT ATTGTGGGGG 1740
GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG GGAGTGTAAG 1800
GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG TATGTGCATG 1860
TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG 1900