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

TagContent
EnhancerAtlas ID
HS145-16998 
Organism
Homo sapiens 
Tissue/cell
NHBE 
Coordinate
chr3:47000960-47003480 
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
chr34700295147003388
chr34700166647002342
Number: 1             
IDChromosomeStartEnd
GH03I046952chr34699369247003318
Enhancer Sequence
ACTCTCACCT GTGTCTTCGG GGTGAGGCCC TCTCATCCCG TGACAAAGGG GTCACATAAC 60
AGATCCCCAC ATTCATGCCT TGTTCCTTCC CTCAGTTCAC CCAGAGCAGC CATCAGTGTC 120
ACCCGGAGGA AGCCCCAGCC CTTGCCCTCG AGCTACCACA GTTGAGAAGA GCAGACCCTA 180
CACGTGTGCA GAGAATATGA ATCCAAGTCA GAAAACGCTA GCCAGTGTGG GGGGACAGGG 240
AGGTGGCAAG GAAGAAGGGC CTTCCACAGA TCATCTTCCC AAATTCAGAC CACCTCCATG 300
CCTGCCTGTT CTGCTCCTGC CCCTCCTCTG CCTAAAATCC CTCCACCTCT TTCACACCTG 360
GAAACAGCTA TCACTCTCCA TGCCATCCAC TCAATCCCTC AAGTGTTTTC TCAGCACCTC 420
TACCAGCTCA GGCTCTGTCT TGTGAGTTAT GCAGCCTGGG ACAAAGCCCA AATGGGGACA 480
CTACTCATAA GCCAACCAAT GAGATAAAGC AGGGTATGTA TATCGATACT GGGTTGAGCG 540
CTCTCCTCCA CGCGACATGC ATGCAAGTGT TGTCCCCCAT CCCCTGTCCA TGCCCTCCCT 600
CCAAGACACT GACAGCTCTC CTCTGCCCCT CCTCCGTGGA TGGCAGTATA CAGTATTATA 660
CCTGGGGGTA CACAGATCAG CCTTCCCACA GGGCCCCAGC CTGACCGTGC TTGAGGCAAG 720
GGCCAGCCTC ACTGACCCCA TTTCCCACCC AGGCTCTGTG CACAGAGAGG CCTCAACAAT 780
AACACTTGTA ACAGCCAGAT GTGGAAACTG ACTCCTCACC CCAGACACAG CCCAGCATTC 840
ACTCTCACTT CCTACATAGA TGGAAGCTGC CTGAGTCATG GACTCCTGGG CCCAGGACAG 900
GAAAGTCCTG CTTTAACCAG ATGATGTCAA ACACAGGTGC TTTTTCTTCA GGATTCAAAT 960
TACCCTGCAA GAAATCTAGT GGTGCCCTGC CCTGAAAACA ATGGGAGGGG GGCTGTCCTT 1020
GAAAGGACAA ATGTTTTCTG CTCCAGCCAC TCACATTTTC TCTAGACAGA GCAGCTCTTT 1080
AGAGCCCTGA ATCAAAACAG CCCAGGAGTG TGGATGTTAC TGCCACAGGG CACCGTTGCC 1140
GAAGCAACTG TTTTTCCTCT TGGAATTCTT TCAAGGATAC AAGCTGTTGC TTCCCTCCAA 1200
AACAAAACCA GGGAGAAGCC AGGGCCCCAG AATTTAAGGG AAAGCTCCGA AGGAAGGAAG 1260
AGGGCCAGGC ATGACTGAGC CTTATCAAGC TCGCTATGGG GTCTCCCAGA TCTCCGAACA 1320
ACTGGCTTAG AAACAGCAAG TCCGTCTCAG CTGCTGAAGG TGTATGTGTA GGGAAAGGCA 1380
AATTGTGGGT ATGGAGGTAT AAAGGTGGTG CTGCTTATGT GTGTTTTGAG GTGTGTATGA 1440
GATATGTATT GGTGTAAAGG GGTTGGGGTT TGTAGGTGTG GGTTGGGGGC ATGTGGAGGG 1500
GTGCTGTGGA GTGTTGGAGG TGTGCAGGGA ATGGGAGGGT GTGGGGAGAA GGGAGGTACT 1560
ATTGTGGGGG GAAGTGTGTG GGGTAGGGCC TGGGGTGTGT GGTGGTGTTG TGAGGTTAAG 1620
GGAGTGTAAG GAGGTGGGAT GCACTGTAGG CAGGGGGCTG GGTGTGGAGA GTACATGCTG 1680
TATGTGCATG TGTATATGCG CTGGAGGTGG GTTGGAGGTA TGTGGGATAG GTTACAGAAA 1740
ATATTCCAAG ATGATATATG AGACATCTTC TCCAGAAACA AAAATATGAA TTGCATTTCA 1800
TTTCTGTATT ACAATTCTTA GTGCTACAGA ATCACATGCT GCTCCCAATG TCTGCAGGGT 1860
CAATGGAAGA GCCAAAAACC ATTTAAAACA TACAGCCCCA GTTTGAAACA ACTGACCCTG 1920
AAGCAACTAT CGGAGGTAAC ACATATTTCT AGTCAGAACA CCCCTGGCTC GGTAGGTCCA 1980
GAGTATGGAC AGAGTCTGGC TAGCAGGTCA GGAGGCCAGC ACTGGAGGGC CTGGCTCAGC 2040
AGGTCCTTGT CTTCCCTGGG AGTCCATGTT GTCTTTTCTC TAGTGCACAA AGCCTAAGGG 2100
GCTCAGAGTC ACAGGACGCA GCATACCCAC TACAGTGCCA TGGGGCACCC AGGAAATGTC 2160
TGAATGTTTT GTTAAAATAA GTTTAAGAGT TGTCTCTGCC TACAAGGAAC TGCCTGTCCA 2220
CTGAAGGGGT GGCATGAATT GGGACTTAGA AGCATGAAAA AACAAATATA TTTTAGCAGC 2280
TACCACTGCT ACTACTACTA CTACTATATG TACAATGACA ATTATCAGGA TGTTATGGAA 2340
GGTTAACAGC ATGATCATAA ACAGTGCATG CCAATTAAGT CACGGGAAAC TCTTCTAAAA 2400
CACAAATGTC AAATATCAAA TAGTGCCAAG TCACTGATAC CCATATGGGG AGAAAAAGAA 2460
TCTTGATCCC TACGCACACC ACACAAAAGT AAATTCGAGA TGGGTTAGAG GTCTAAAGGT 2520