EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-00398 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr1:8497320-8500120 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs34976449chr18498327hg19
rs301803chr18498680hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELF3MA0640.1chr1:8498713-8498726TTACTTCCGGCTA-6.54
ONECUT1MA0679.1chr1:8498368-8498382AAAAAATCAATATA+6.62
ONECUT2MA0756.1chr1:8498368-8498382AAAAAATCAATATA+6.91
ONECUT3MA0757.1chr1:8498368-8498382AAAAAATCAATATA+7.19
Sox6MA0515.1chr1:8499620-8499630CCATTGTTTT+6.02
Number of super-enhancer constituents: 30             
IDCoordinateTissue/cell
SE_00045chr1:8497982-8499894Adipose_Nuclei
SE_02022chr1:8497126-8497782Aorta
SE_02022chr1:8498913-8499948Aorta
SE_03947chr1:8498778-8499975Brain_Anterior_Caudate
SE_04978chr1:8498182-8500162Brain_Cingulate_Gyrus
SE_07042chr1:8498385-8500215Brain_Hippocampus_Middle_150
SE_07921chr1:8498882-8500242Brain_Inferior_Temporal_Lobe
SE_11329chr1:8496575-8500743CD20
SE_25808chr1:8497845-8499987Duodenum_Smooth_Muscle
SE_28078chr1:8498322-8500011Fetal_Intestine
SE_29095chr1:8498172-8499988Fetal_Intestine_Large
SE_29887chr1:8497659-8500219Fetal_Muscle
SE_31622chr1:8498048-8498478Gastric
SE_31622chr1:8498521-8499967Gastric
SE_40658chr1:8498953-8499664Left_Ventricle
SE_41679chr1:8497482-8498209LNCaP
SE_41679chr1:8499010-8499949LNCaP
SE_42166chr1:8498911-8499835Lung
SE_48103chr1:8497785-8498257Psoas_Muscle
SE_48103chr1:8498317-8498850Psoas_Muscle
SE_48103chr1:8498931-8499864Psoas_Muscle
SE_48600chr1:8498898-8499546Right_Atrium
SE_51176chr1:8496821-8497964Skeletal_Muscle
SE_51176chr1:8497978-8500178Skeletal_Muscle
SE_53408chr1:8499004-8499850Spleen
SE_54752chr1:8497250-8500103Stomach_Smooth_Muscle
SE_58576chr1:8455425-8501956Ly1
SE_60225chr1:8480836-8499894Ly4
SE_60758chr1:8454848-8500160DHL6
SE_62661chr1:8450826-8509851Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr184985928498880
Number: 1             
IDChromosomeStartEnd
GH01I008437chr184976518500633
Enhancer Sequence
TGGGACTGGG TTCCTCATTT GACTCGGTTC ATTTAAAGAA TGATCTCAAA GAAGAAAGGA 60
AAATCAATGA CCCCTTTAGG AAATGTAGTC CAGGGTGGGG GTGGAGGAAG CATTTCAATG 120
ACAAAAGCCA AACCTCAGTC ATAATGCAGA TCCCTGTCTA ACAGGTGATC ATTGTTTTTT 180
TTTTCTATTA CAGGCACTCT GGTCTCCCGC CTACCCCATG CAGGATGGCT ATCCCCATGC 240
AGAATGGCTG TGACTTTCAA GAGAGTCCCC CAAGGGAGGG TCCCAAGATC AGGGGCTGGT 300
AATGGGCCCC ACCACAAGGC TACGCTGCTG GCTTTTGTTT GGAACAATAG CGCTCCCATG 360
ATACCTCACT CTTGCTGACA ATATTGGTAA TACGGGAGCA TGAACACAGC TGTGTGTAAA 420
TTACACACAC AAACAGATTA GATCTGTATA TTTATAAGGA ATACAAACAT ACTAATAGCT 480
CATTTACATA CACAGCTGGA TACAATGGGC TGCATGCAGA GGGGAGTTTG AGTTCCAAAG 540
TATTTCTCTA AAATTTTACA AAAAGAAATG CTCAGATTAC TGCTAACCCA GGCTGAGACT 600
TCTGCTCCCC CCACCCCCAT GCAGTATGTC CCCCGAAATA GAGTCCTTTT CATCCTCGTT 660
TGTGATATTT GAGATGCTAT GAAGGAGAAA CCTCAACAAG TGCTGTTAGA TTTCACTTTT 720
ATTATTATTT ATTATTATTT TTAGAGACAG GGTCTTGCTC TGCCACCTAG GCTACAGTGG 780
TATGATCACA GTTCACTGTA ACGTGGAGCT TCCGGGCTCA AATGATCCTC CTGGCTCGGC 840
CTCCCAAGTA GGTCAGACTA CAGGTATGTG TCAGTTACCA TGCCCAGCTA ATTTTAAAAA 900
TATTTTTTTG TAGAGACGGG GTTCTCACTA TGTTGCCCAG GCTTGGTCTT GAACTCTTGA 960
TTTCAAGCAA TCCTGCTGCC TCAGCCTCCC AAAGAGTTGG GATTATGGCA TGAGCCACTG 1020
TGCCCAGCCA GATCTCACTC CTGTAGGAAA AAAATCAATA TAGGATAATT TTCAGTTAAA 1080
AAGATGTATA TACATACGAA GAGGGAGACC TACTAAAACA TCTGTTACAA CAGCATATAG 1140
TAAGGCAGAA TCTTTGCATT TTCAAAATGT TTTCATAAAC TTTATTTGTT AGAGCAATTT 1200
CAGGTTCACA GCAAAACGGA ACAGAAGGTA TAGGGATTTC CCATATAGAT GGGTCTCTGG 1260
ATTTTTCAGC TAATTTTGAA AAATAGGGAA AAGAGCAATC AGCATTTTGT GCTCACTACA 1320
GTAAACCAGG AACACAGGCA TCAGGAGAGC TGGGCTCTGA TTCAAAGGCC TGATTCTAGC 1380
AAGGCCTCAC AGTTTACTTC CGGCTAGCCA TGAACACTCT CTGCGCCTGA GGTTTTCGTG 1440
GAAAGACAGC ATCACAAGTA CTCAAATGTA GCGTTTAAAA GTACTAACTT TTAAAATGTT 1500
GAATGTTCCA GTAAAACAGT TAAAGAAAAA AAAAGGTAAT AATCCAACTA AGTAAAAATA 1560
TTAACTTATA CATATCTGGA TAGATGATAA GCTCATTACA GGCCCTAATT TTATTATTTA 1620
AAATGTTTAC AACAAAACTC TCTAATTGAT ATTCTCCCTC TCTCTCTCTT TTTGCCTTGA 1680
TATGGTTTCT ATAAACTCTT GGTTTAAAAA AGAAAAAAGG TCCATTTCTG AGGCTTGGGT 1740
TTACTGTACT TACAGTTCCA CCAGTAAATC GTCTCCCAGT CTGGGCTGGA GAAGCGCTGG 1800
CCACGGTTTG ATTGCTCCAG CCCCAGGTTG CCAGGCAACC CACACAAGGG GGAAGTCTGA 1860
GAACCGCTGA CAGATAGCCA AGTGGCTGAA ACAACAGACT TCTCTCTGTC AAAAATGTGT 1920
TTGAGAGAGC CACTTGCCCA CCTCTGCTCT CTGCTAAACA CTACATGATT GTAAAATCAA 1980
AATCAAAAGG CCACTGTAAT AAAAACACAC TTCCTGCTCA ATTACTAATT GTTCTAAAGC 2040
TGTGGGGAGG CCCAGATCCT ACAGTGTATG GCAACAGAAA TGCGATACTG TAAATGAGAT 2100
AAAGCCAGCA GCATGCAAGA AACCTGATCT AAATGCATCT CCGTAGCTTC AAGTCAGGAG 2160
AGCTGGTGTG TGGAGGAATC AACTGCCTAA GAAAACACCA GGAAGAAAAT AATGAATGTC 2220
AAGATGTTAA AGAAACAAAC CAATCAATAA CTACGAAGCT AGAGGTCAAG ACTACTTAGT 2280
AATAAAACCA AGAACATTCT CCATTGTTTT GAAACACAAT CTGGAGGCAA TGAAAGTTTT 2340
CTCCCTCAGA TGGAAAGGAG GAGCAAGAAA GGTCAATGAC CCTTGGGAAC CACACCCCCT 2400
GGCGGTTCCA GGTGGATTCC CTGATACTTG ACTGTAAATG GGATTACAGG AAATAGTAGC 2460
ATCCTTAGGA TAATGCAGGA CAATAACAGG TCTGAGAGTC TAATGCAACA TTTAAAATAC 2520
CTATGGTGTG AGCTGGGCAC AGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCGA 2580
GGTGGGTGGA TCACCTGAGG TCAAAAGTTT GAGACCAGCC TGGCCAACAC AGTGAAACCC 2640
CGTCTACACT AAAAATACAA AAAATTAGCT GGGCATGGTG GCAAACGCCT GTAATCCCAG 2700
CTACTGGGGA GGCTGAGGCA GGAGAATTGC TTCAACCCGG GAGGCAGAGG TTGCAGTGAG 2760
CTGAGATCGC GCCATTACAC TCCAGCCTGG GCAACAAGAG 2800