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

TagContent
EnhancerAtlas ID
HS104-06034 
Organism
Homo sapiens 
Tissue/cell
HUVEC 
Coordinate
chr1:234852780-234854780 
SNPs
Number: 3             
IDChromosomePositionGenome Version
rs556107chr1234853059hg19
rs557933chr1234853268hg19
rs558971chr1234853406hg19
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
LMX1BMA0703.2chr1:234853267-234853278ATTTTAATTAA+6.62
POU2F2MA0507.1chr1:234854335-234854348ATATGCAAATGAG-7.52
Pou2f3MA0627.1chr1:234854333-234854349AGATATGCAAATGAGA+6.06
ZNF263MA0528.1chr1:234853930-234853951GGGGGAGGAGAATGAGAAAGA+6.97
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_01816chr1:234851920-234853206Aorta
SE_01816chr1:234853269-234862739Aorta
SE_03123chr1:234851948-234853100Bladder
SE_04206chr1:234851848-234864664Brain_Anterior_Caudate
SE_05210chr1:234852339-234866021Brain_Cingulate_Gyrus
SE_06159chr1:234851621-234865554Brain_Hippocampus_Middle
SE_07154chr1:234851931-234854072Brain_Hippocampus_Middle_150
SE_07154chr1:234854316-234864617Brain_Hippocampus_Middle_150
SE_08108chr1:234852036-234868294Brain_Inferior_Temporal_Lobe
SE_23501chr1:234850856-234854176Colon_Crypt_1
SE_24081chr1:234851981-234853206Colon_Crypt_2
SE_24081chr1:234853299-234854253Colon_Crypt_2
SE_25941chr1:234850948-234863804Duodenum_Smooth_Muscle
SE_26800chr1:234850930-234853175Esophagus
SE_26800chr1:234853287-234854156Esophagus
SE_27714chr1:234849701-234863899Fetal_Intestine
SE_28624chr1:234846479-234863924Fetal_Intestine_Large
SE_29677chr1:234852242-234854916Fetal_Muscle
SE_31598chr1:234850948-234853235Gastric
SE_31598chr1:234853251-234854300Gastric
SE_33532chr1:234851300-234853496H2171
SE_33532chr1:234854224-234864870H2171
SE_38136chr1:234852748-234863540HUVEC
SE_40926chr1:234850897-234863890Left_Ventricle
SE_42335chr1:234851052-234854297Lung
SE_42335chr1:234854497-234864876Lung
SE_45839chr1:234853647-234863630Osteoblasts
SE_47018chr1:234852767-234853150Ovary
SE_47205chr1:234851968-234863960Panc1
SE_47784chr1:234853336-234853613Pancreas
SE_47784chr1:234853617-234854013Pancreas
SE_48724chr1:234851922-234853176Right_Atrium
SE_48724chr1:234853296-234854346Right_Atrium
SE_48724chr1:234854580-234862831Right_Atrium
SE_50295chr1:234850736-234862837Sigmoid_Colon
SE_51414chr1:234851031-234863972Skeletal_Muscle
SE_52508chr1:234850914-234854694Small_Intestine
SE_54175chr1:234853308-234854440Spleen
SE_54631chr1:234850764-234864075Stomach_Smooth_Muscle
SE_58214chr1:234854291-234859985VACO_9m
SE_61992chr1:234850904-234881356Toledo
SE_63435chr1:234845326-234887436NCI-H69
SE_65556chr1:234851662-234853082Pancreatic_islets
SE_65556chr1:234853329-234855159Pancreatic_islets
SE_66916chr1:234854224-234864870H2171
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1234853034234854774
Number: 1             
IDChromosomeStartEnd
GH01I234714chr1234849979234864746
Enhancer Sequence
ACCCAGACCC GAGCTCCGTA ACTGCTCTGG TATAGAGCTG GGCTCTGTGC TATGGAGACA 60
GTACTGACAT TTCATCTTCC CGAGGCACGT CCCCTGGCTC CGTGATGTGG CCGTACAACA 120
AGCCTGCCCT TTGTTACGGT GTGTGCACAC ATGTAAGTGC TCTCGACAAA TCTGTGTTCC 180
TGCCTCTCCT CCAGTGCTTC TCAGGCAACG ACGTTACCCT TGGCCTCAAG GAAAAAAAAC 240
AGACACCGTT GGTTGGAGAT TACTGAGTAA ACCTACAACG TCCTCATGCT TAAGGCCCCG 300
TCTGTGATTC CACCATGAAG GTCACATATC CTCTCTCCTA AAAAGACCTC ATGTCTCCAT 360
TTAAGTATTT GTTTGGGAAA ATGCTGTATT GTATTGAAAT TATTGTATAA AGATAGGGCC 420
TTGGTACAAA ATCTAGGAAT GTGAGGTTTA AACACAGTTG GATAAATTTT TAAAAATCAC 480
ATTGCAAATT TTAATTAAGG CGAGGGAGCT TAATTTAAAC AAATAAATGA TTAGTGTTGA 540
CTACCAGAGT ATAAACAAGA CTGTAGTTTT AAAATGTAAT CAGCGTTCTC CCCATTTTCA 600
GACATTATCC TGGTCTGAAT TCCTCACCCT GTCCTCTCTT TGCAACACGA GGCACAGTGA 660
GCTGTGGTCT GGACTGTTTT TGCAGCCCCT CTTTGGCGAC AACAGGGTAG AACCCACAGC 720
CATCAAATCA GCCTCTAGGT TGGCCCAAAA CATCACAGTG GCCTGGACAT GATGGAGTAT 780
TTCCAGGCAC ATAGAAACTT GGCCTTTATT CTTCCGGGTT GTAAATCTGG CACCTCTCAG 840
GATCAGTAAA TAAGCTTTTT TAAAAGCCCA AACAAACCAT AAGGAAATCC TGCATTCTGA 900
AACAAAAGGT ATGAAAGCTA AGTCAAGACC CACACTGCCA TTGTGTCACT TGCCAGGATG 960
TGAGCTGCTG CCTTGGGAGA AAGATAACAT GAAAGAGGCT ATAATTGCAG GGCTGAGACT 1020
CCAGGTCCCA TGAAAACAGG ATAAAAAATA GCAAGCAAGA AGTGTTCCCT GAGCTTTCAG 1080
CTGGGCTAGG GTGGGGAAAA AAATCAAAAG AGCAACACTC TCCTGAAGTT GTTCAAGAAA 1140
TGGAGACACA GGGGGAGGAG AATGAGAAAG AACACCAAGG CCAAGTTAAC GTGTTTAGGA 1200
AAAATATGGG GGCAGGAGAG AAAAAAAAAA AAGGCGGAAT GATTTAATGC CAGCCAAAGT 1260
AACTAAGGGG AAGAAGGTGT GTTTTTATAA ACATGTTTGC TTTTGTGTGT GTGTGTGTGT 1320
GTGTGTGTGT GTGTGTGTGT GCCGGGGGAA AAGTGTGGAA AAAGAGAAAC TAGGTCCATT 1380
AATGAAGGAG TAGGGTGTTG CAAGGGAAAT GACTAAATTA GCTGAGCTTT TAAACTGCTT 1440
TTAAAAAATT AGCTTAAATG AGAAAAATAA AGATAAGAGG TAAGAATGAT TGGGAGGATG 1500
CAGTCAATAA ACTATTGATA AGGAAGGGTT AAAGGAGTAT TTAGAGAAAT TGAAGATATG 1560
CAAATGAGAG GTCAAAATAA CAGTAGCCCA GTGTAGTTAG TGGAACTAGC TGAAGAATTT 1620
GGAACACCAC GGCGGGACTT CATAACCACT CAGTCTACAG GGAGTACTAA GAACACATTC 1680
TAACATTGTA CAGCACCTTA TACTAACATT GTGCATGATA AATGCATTCA TTGTTCTCAC 1740
ATTCTTACAT TCATCTGAGT CTGGTCTTTA CCTCCACTAT CAGCAGCAAT GTGATAGGAC 1800
TGACCAAAGC GAAAGATGTT TAAAACTCTT TTTGGTATGA AACAGAAGCA AAATCACTTC 1860
TCTCGGTAAT AAAGAAGGAC ATTGAGGCAT TGAGTAGTCA AAGGAATTGC TGAAGATGAA 1920
ACACCAAGTC AGTGACTAAG TTCTGACCCA TTTTTAAGAA TTCAGACATA TTCCCCCAAA 1980
AAGAAAGAAT GTATTTAACG 2000