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

TagContent
EnhancerAtlas ID
HS051-22627 
Organism
Homo sapiens 
Tissue/cell
Fetal_thymus 
Coordinate
chr5:172191620-172194210 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs114503346chr5172192350hg19
rs322353chr5172192868hg19
TF binding sites/motifs
Number: 5             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
JUNMA0488.1chr5:172192582-172192595ACAATGATGTCAT+6.33
JUND(var.2)MA0492.1chr5:172192581-172192596CACAATGATGTCATC+6
RUNX1MA0002.2chr5:172192749-172192760AAACCACAGAA-6.32
ZNF263MA0528.1chr5:172192694-172192715GGAGGTGGGGGAGGGGGAGTG+6.67
ZNF263MA0528.1chr5:172192691-172192712GGTGGAGGTGGGGGAGGGGGA+7.61
Number of super-enhancer constituents: 69             
IDCoordinateTissue/cell
SE_00085chr5:172191130-172206161Adipose_Nuclei
SE_00944chr5:172191973-172194206Adrenal_Gland
SE_01555chr5:172191429-172195212Aorta
SE_02290chr5:172191680-172201450Astrocytes
SE_02948chr5:172191989-172194194Bladder
SE_04740chr5:172191492-172198322Brain_Anterior_Caudate
SE_06342chr5:172191421-172203095Brain_Hippocampus_Middle
SE_07406chr5:172191544-172201084Brain_Hippocampus_Middle_150
SE_09032chr5:172192924-172194077Brain_Mid_Frontal_Lobe
SE_09165chr5:172191139-172206360CD14
SE_10246chr5:172191509-172194277CD19_Primary
SE_11134chr5:172190121-172202303CD20
SE_11865chr5:172191236-172194207CD3
SE_12991chr5:172191412-172194109CD34_Primary_RO01480
SE_13477chr5:172190646-172194202CD34_Primary_RO01536
SE_14194chr5:172191239-172194330CD34_Primary_RO01549
SE_14398chr5:172190420-172202581CD4_Memory_Primary_7pool
SE_15453chr5:172191522-172193642CD4_Memory_Primary_8pool
SE_15826chr5:172191242-172194095CD4_Naive_Primary_7pool
SE_16328chr5:172191549-172194061CD4_Naive_Primary_8pool
SE_16888chr5:172191380-172194437CD4p_CD225int_CD127p_Tmem
SE_17423chr5:172190321-172201820CD4p_CD25-_CD45RAp_Naive
SE_17830chr5:172190464-172201683CD4p_CD25-_CD45ROp_Memory
SE_19397chr5:172191268-172194271CD4p_CD25-_Il17p_PMAstim_Th17
SE_20021chr5:172191433-172201669CD56
SE_20749chr5:172191297-172201296CD8_Memory_7pool
SE_21466chr5:172191380-172194313CD8_Naive_7pool
SE_22011chr5:172191368-172193986CD8_Naive_8pool
SE_22407chr5:172191271-172194286CD8_primiary
SE_23118chr5:172191464-172194226Colon_Crypt_1
SE_23781chr5:172191483-172193973Colon_Crypt_2
SE_24715chr5:172191455-172194341Colon_Crypt_3
SE_25789chr5:172191223-172206431Duodenum_Smooth_Muscle
SE_26519chr5:172191437-172203709Esophagus
SE_27813chr5:172191412-172207743Fetal_Intestine
SE_28860chr5:172191515-172195241Fetal_Intestine_Large
SE_29599chr5:172191456-172201187Fetal_Muscle
SE_31376chr5:172191389-172195236Gastric
SE_34653chr5:172190369-172206553HeLa
SE_36186chr5:172191226-172200824HMEC
SE_36923chr5:172191402-172202832HSMMtube
SE_38185chr5:172191227-172201096HUVEC
SE_40610chr5:172191399-172201635Left_Ventricle
SE_42186chr5:172191447-172205889Lung
SE_44221chr5:172191438-172206056NHDF-Ad
SE_44768chr5:172191597-172201545NHLF
SE_45880chr5:172191429-172206262Osteoblasts
SE_46940chr5:172191965-172193957Ovary
SE_47360chr5:172191383-172198291Panc1
SE_47554chr5:172192002-172194263Pancreas
SE_48206chr5:172191408-172202951Psoas_Muscle
SE_48563chr5:172191509-172201630Right_Atrium
SE_49710chr5:172192039-172193130Right_Ventricle
SE_49710chr5:172193145-172194029Right_Ventricle
SE_50124chr5:172191420-172195248Sigmoid_Colon
SE_51114chr5:172191158-172203545Skeletal_Muscle
SE_51800chr5:172191782-172201742Skeletal_Muscle_Myoblast
SE_52338chr5:172191437-172207121Small_Intestine
SE_53284chr5:172191476-172206463Spleen
SE_54705chr5:172191090-172201809Stomach_Smooth_Muscle
SE_55249chr5:172191958-172194075Thymus
SE_55716chr5:172191796-172194024u87
SE_58018chr5:172191912-172192555VACO_9m
SE_61533chr5:172191523-172278016Toledo
SE_62363chr5:172184582-172235488Tonsil
SE_63680chr5:172191782-172201822HSMM
SE_64975chr5:172191439-172200111NHEK
SE_65260chr5:172190258-172196593Pancreatic_islets
SE_67508chr5:172191796-172194024u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr5172192263172193766
Enhancer Sequence
CTTGAACGCA GGTCTAGCCA ACTCCAATTC ACACGCTGTA TCCACTGGTC CACAAACATA 60
CCTCTCAAAC ATCAGGTCTT TGCTGCTCTC CTGGCCTTGG AGCCCTCTTT CCAGTTCACC 120
TCTCAAATGG GCAACTGGGT TATATCATTC AGGTCTTAGT TTATCCTGCC TTCATAGCCT 180
TCATCCTTAT CTTATTTTGT GATTATCTTA TTTCTATAAC CCACCCATAT ATAGTGCCAT 240
GAGACGGCAA GTGACAAAGT AAAATTACTT TTGCTGTTTA GCGAAAATAG CAAAAGTAAT 300
TTTAGCTACT TATAAGTAGG AATTTTGTCT TGCACCAAAG TATCCCCTGA GACTATACTT 360
ATCAATATTT GTTGAACACA TGAATGAATG AATGAATGAA CGAATGAGTG AATGAATGCG 420
TGGGCCTCCT GCCTAGCTTT AAAAGCCACA TTCAAGGAAA AGGTGGCTAT GAGCTTATCT 480
TCCTTGGCAG AGCAGTTTTG TCCACTGTGG CGCTAGCAGA GAGCACACCC TTTGTTCTCC 540
ACGGGGTGGA AGACACCTCC TCGGTGGGCA GAGGGGAGCA GGGCTGCTGG TCTGCACCTA 600
CAGGCTGTTC TCAAACAGGC TCACCCCGCA GAGCTCTGGA AACGAGGTGA GCAGCCCTCC 660
CACCTGCTCT CCAGAAAGCA ACCTGCAGAG AAAAACAGCC CGGGTTGACC TGGATCCACC 720
CGGCGGGCGC GGGGAGGGGC CGCAGCGGCA TTGTTTGCCT CTGTGTATGG CAACCAGAAA 780
CCACGGCAGC CAGCACTTCT CAGAGGCACC CCGCCCCCCT TTATTTTAAT CTCCTAAACT 840
GATTTGTCAG CAGCAGGAAG TGACATGACA GCTTTCCTCA CAAAAGGGAA ACTCCTCCGC 900
GTTACCATGG GGATGGAGGC CACTGTAGGA TCACAGATTT ATATAATCTT AAAGGTGTAC 960
ACACAATGAT GTCATCCTCT GACGGGCCAG GGGAGGGAGG GAAAGGGACG CCAGAGGCTG 1020
CAAGTCCAAA GCAAATTAGC TACGATTTGC AAAATTCCAA GGAGAGGATG CGGTGGAGGT 1080
GGGGGAGGGG GAGTGTTAGA GGTATTATAA TGAAATAATG GGTGCCTGGA AACCACAGAA 1140
AAGCATAATG TATGCATTGA TGCATTTTCT ACATCCCAGA ATTAGAGAGA TGGGAAGAAC 1200
AGTACTCAGA TCCAGTGCAA ATTGGTCATT TTACGGGGTG GGAAAACTGA GCCAGAAGAA 1260
CTGCCAGAAG CCATTAGGAC AGAGACAAGG GGATGGAAAC ATTTCTCCAC GGCCCACTGT 1320
GTGCCAGGCA CTTTACATTC ATCAGCCCAT GTCTTTCTCA CAAGTGAGCC TCAGTTTTGT 1380
CCTCTGTAAA ATGGGTATTG CTGTCAAAGG TTACTTAACC TTAGCAGTAC CTGGCACACA 1440
GTGCTCACTC TAAAACTGGC AACCATCATT GCCACATTAT CAGTATTAAA AGTCTTATTT 1500
CAATCTCTTC CTGGGAAACA CATTAATAGA CTTTAAGTAT CTTTCATCAC GAGGTATTAA 1560
TTTTTTCCCA AGGAAAGCAG TCTGAGGCCA AATATGAGAT TTTTCTGGAG GGTCTGAACA 1620
CAGTGACTCC GGTACATGGG GATCAGGGGT CATCATTCCT GGCTCTCAGG GCTGGCATGA 1680
GGCAGAGTGG CTTGAGCCGG GAGAAGTGAG TGACTTGTTT TCACTGGCGG CTCCCTTAGG 1740
CAGCCGCTGT ATTTTTCCAC TGCGTGGATC ACACTGGAGA TTAATTTTGG TTCAGCCAGT 1800
GCCTGCCAAG CAGAAAGCGA AGGCCCTAGC CCACGGGGAA GTCAGCCATG GCATCTGTCA 1860
CAGACTCGAT GTCGCTGGTA CATTTCCACG GAGAGAGATA TTTACAATAG TAAATTTCTA 1920
GGCTTTGATA AAAACACTGG GTACGATTTG TTTTGATAGG CATGAACATA CTTGTAATCG 1980
GAAACCCAGC TGAGGAAATG AGCTTGCCAG CCCAGGGTAA GTTCTTAGAA CTTAGAACAC 2040
AGGGATCTTT CAGACCCTGG GAGTCAAGTG GCAGACAGTG AGCCACAGGG GCAAAGTCAA 2100
GGACACTGAT TCTGCGTAAA GACCTTGAAC AACAGGACAG GACCAGAACC ATAGCACAGG 2160
GTGCTCATGG ATAAGGCGAA TGGGATATTT CCTTTTCTGC TTCCCATAGC ACTTTGTCCA 2220
GAAACAAAGA GTGGGGTGGG GCGCTAAGGG GCCAGTAATC CAAGAGCTTC GCTGTTTCTT 2280
AACGCAACAT TATAGACTGG ATTATGGATT GGTAGCAATT ACATCTCTTC TGTTTTTTGC 2340
CTGCTTGGCA AAGGAGTACA AATTCAGAAT ATTATCCTAG AACAAGTCAG GTTTAATTGC 2400
TTATCTCAAC AAAACTATGA AATCAGAGCA GCAGGTGACA TGAAGGAGGC AACTACCAAA 2460
AATGCCATGT CTATATGCAG AAATGCCAGC GTGAATGTCC TCCACAATGT TAGCAATGGT 2520
CAGGTTGGGG ATGGGCTGTT GCGGGTGATT TCTTTACATG GTATTTGCTT ATAGTGCTTG 2580
GATTTTTTTT 2590