EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS050-55424 
Organism
Homo sapiens 
Tissue/cell
Fetal_stomach 
Coordinate
chr5:131801460-131803690 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs2522056chr5131801726hg19
rs17622517chr5131803537hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ESR1MA0112.3chr5:131802673-131802690AGGCTCACAGTGACCTT-6.07
ESR1MA0112.3chr5:131802673-131802690AGGCTCACAGTGACCTT+6.28
EsrraMA0592.2chr5:131801817-131801828ATGACCTTGAG-6.02
EsrrgMA0643.1chr5:131801817-131801827ATGACCTTGA-6.02
LBX2MA0699.1chr5:131803142-131803152GCCAATTAGC+6.02
SPI1MA0080.4chr5:131803547-131803561CACTTCCTCTTTCT-6.51
ZNF263MA0528.1chr5:131803551-131803572TCCTCTTTCTTGACCTCCTCC-6.55
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_00037chr5:131801669-131804171Adipose_Nuclei
SE_01257chr5:131801990-131803186Adrenal_Gland
SE_09163chr5:131799339-131804166CD14
SE_10340chr5:131801416-131804001CD19_Primary
SE_10915chr5:131798063-131818030CD20
SE_11856chr5:131798507-131804031CD3
SE_13479chr5:131798645-131803817CD34_Primary_RO01536
SE_14495chr5:131799289-131803905CD4_Memory_Primary_7pool
SE_15423chr5:131801470-131803698CD4_Memory_Primary_8pool
SE_16304chr5:131799078-131803878CD4_Naive_Primary_8pool
SE_16894chr5:131801586-131803325CD4p_CD225int_CD127p_Tmem
SE_17370chr5:131798295-131804719CD4p_CD25-_CD45RAp_Naive
SE_17764chr5:131798263-131803976CD4p_CD25-_CD45ROp_Memory
SE_18258chr5:131797949-131803992CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131799050-131803746CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131797758-131816289CD56
SE_20775chr5:131799136-131804086CD8_Memory_7pool
SE_21523chr5:131801353-131804093CD8_Naive_7pool
SE_21960chr5:131799223-131803779CD8_Naive_8pool
SE_22284chr5:131797996-131818026CD8_primiary
SE_23750chr5:131801530-131801831Colon_Crypt_2
SE_23750chr5:131802106-131802595Colon_Crypt_2
SE_23750chr5:131802611-131803049Colon_Crypt_2
SE_25340chr5:131788298-131808279DND41
SE_25784chr5:131798529-131803921Duodenum_Smooth_Muscle
SE_26597chr5:131801478-131803762Esophagus
SE_27629chr5:131801861-131803896Fetal_Intestine
SE_28559chr5:131794264-131804122Fetal_Intestine_Large
SE_30917chr5:131801446-131803985Fetal_Thymus
SE_31393chr5:131801508-131803785Gastric
SE_37771chr5:131798722-131803794HSMMtube
SE_39368chr5:131801472-131803972Jurkat
SE_40726chr5:131801506-131803006Left_Ventricle
SE_42103chr5:131801441-131803807Lung
SE_43869chr5:131798062-131804366MM1S
SE_48659chr5:131801638-131803058Right_Atrium
SE_50023chr5:131801484-131803967RPMI-8402
SE_50051chr5:131801459-131803972Sigmoid_Colon
SE_52336chr5:131797662-131804003Small_Intestine
SE_53285chr5:131797984-131804080Spleen
SE_55171chr5:131801470-131803793Thymus
SE_61818chr5:131790756-131837647Toledo
SE_62219chr5:131721125-131837948Tonsil
SE_66244chr5:131801472-131803972Jurkat
SE_67186chr5:131798062-131804366MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr5131801987131802854
chr5131803262131803600
chr5131802496131802987
chr5131801595131801732
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
AGAGACGGGG TTTCTCCATG TTGCTCAGGC TAGTCTCGAA CTCCCAACCT CAGGTGATCC 60
ACCCACCTCA GCCTCCCAAA GTGCTGGGAT TACAGGCATG AGCCACCGTG CCGGGCTGAC 120
AGTGGTTTTT AAAGGGGGAG GGCAGATGAA GGACGTTGGT GGACCATCCT CTGGGAGGAG 180
ATGTGGACTG AGGAAGCAAC GCTGACCTCA GGCCCCACAC CACCCTTTCA CCTCAGCCTC 240
ACTTTCTCAT CAGTAAATGG AACTCGTTCT TGTGTATGTG CCATGGAGGC AATGTAGCAG 300
AAGAGAATAG GGCAGACTTT GGAACTCAGC CATCTGGGAG AAAATCCTAG TTATGTGATG 360
ACCTTGAGCC AATGACTGAA TTTCTCTGTC TCATTTTCTC TTCTGTAAAA TGGGGACAAT 420
TACAGTGAAT TCTGTGAATT CATTCATGTC CCTGACACAT GGTGTGAGCT CAGTCATTAC 480
CTTTGCGAGG GTTGCAAGGA TGTAATGAGA TGGCAGATGT GAGCACAGCT CCCAGACCCG 540
AAGGTGCTGT ATGAATGGGA GGGAGCAGTG AGTGTTATTT GGGAAATATT GAAGACACAA 600
CTTCCCTCCC ACATTTGTCT GGGGTGGAGC AACAGTTTTA CTTATTTAAT GATAAGCTGG 660
AAGATGCACC AAAGGGAGGT GAAAAACTGA AACCGCCAAC CGTTTGAGCT CCAGGCTGCA 720
CCGAAGCGGT GTGGCTGGTG CAGATGGTGA GAGCCCCAGT GCCGGCCCAC TTCCTCCATG 780
AGTGCCACAC GCCTTTCTCA AGCTAGCCGG CTTCCCAAGG CTGCAGGAAG TGGGGCCAGG 840
AACAGGCCCT CCGGCTGTGT TGGGGGAGGC CTGGGCAGGG GTTGGCAGCT GCTGGGTGTG 900
AACGGAAGTC TTGGAGGTCC TTGAAGGTCC TGGGGCCGCC TGCACAGCAG CCCCTGCCCT 960
CTCCCTGTCC AGGCCTGCCC AGGACTAGCT TGTAGCAGAC TCTTCTTGTA GCCTAGGCTC 1020
TTGCCTCTTG CAGTAGTGAG CCATTGTACA AAAGACATCC AGCGGAGGGA GGCAGGCTGG 1080
AGAGGAGGAC AGCCGAATCT TTTCTCAAAG GAAATGCAGT TGTGGTTTTG AGACGTTCAT 1140
ATTTCACATC TGTGGTTGGC GTTTCCCAGG GTTCTCAGAG GTGAATGCAG GGTCAGCCCT 1200
GTGTCACCAA ATAAGGCTCA CAGTGACCTT AGCAACAAGC TTTGCTGCCC ATTGGCTGTC 1260
ACTGCTGCCG CCTGCCAATG CGGCCTCCTG AAGGCCAGCA CTGATGCTGA GCTGAAACTT 1320
CTGCATGTGC CAAGGTCCAG CTGCCTCTGT CAGAAATCAC CGTCCTTGGA AGCAGCCACA 1380
GATAGGTAGA GAGCTCCGGA CAAAGGTGGA CAAGGTCAGT GGGAGGACTG TCCAGGTGTC 1440
CATGTTTCAG AGTCCACCTG GCCAGCATTC CATTCTCACA TAGCACCAAA CCAGCACCTT 1500
GGTGGCCTGG TCCCAGCTTG CCAGGACAAC CCCCCATTCC ACCCTGTCAA CCTTGAACTC 1560
TATAATGGTC ATCATTTCAT AGCTCTGCTC ATTTTAGTTC CACTGGGTTC TCCCTTGTGC 1620
TTGGCACTTG ACTAAGCTCC TTCTACACAT TACATCTTTT ACCTCTCTCA ACAACCCTGT 1680
GAGCCAATTA GCCCCATTTT ACAGGTGCAG AAACTGACAC CAAAGGAAGT CAGTAATGGC 1740
CCAGGTGACT GCACCACTAG TAAGTGGGGA AGTCAGAATT TAAACCCAAT TTAAACAGAC 1800
CTAGATCCCA TGCTATTAAC CATTGCACTG TATTGACAGA CACTCAATGT CCGTGCAGCT 1860
CAGTGTCTTC ATTCTGTGAC ATGGGGATGA CAGTACCGTA CCTCACAGGG TTGGGGTGAG 1920
CATTGTGTGG AGTGACTTAT GTCCAGAAGC ACACCTTTGC ACCAGTGGCC TTGGCACCCC 1980
CAAGGCATGC TCCACAAACA GCTTGCACAT TCCTTTCTCA CAGCGTGTGC TGCTGAAACA 2040
TTGAGGTTTG TGGACCGGAC TTCTCTGTAG CCCTTGTATT TAGTTTTCAC TTCCTCTTTC 2100
TTGACCTCCT CCCACCCCCC ACCCAACTGC AAGGTAGGGA GGCTACTGAG GGGCCAGCCT 2160
GTGGATTCCA GAGGGCACAG GGCTATCTGG GATGGAGGGG ACAGGGTTCT GAAGACAGAA 2220
GGTGGGAAGG 2230