EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS095-24645 
Organism
Homo sapiens 
Tissue/cell
HMEC 
Coordinate
chr5:131801620-131803730 
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: 3             
ChromosomeStartEnd
chr5131801987131802854
chr5131803262131803600
chr5131802496131802987
Number: 1             
IDChromosomeStartEnd
GH05I132452chr5131788089131817782
Enhancer Sequence
GGACCATCCT CTGGGAGGAG ATGTGGACTG AGGAAGCAAC GCTGACCTCA GGCCCCACAC 60
CACCCTTTCA CCTCAGCCTC ACTTTCTCAT CAGTAAATGG AACTCGTTCT TGTGTATGTG 120
CCATGGAGGC AATGTAGCAG AAGAGAATAG GGCAGACTTT GGAACTCAGC CATCTGGGAG 180
AAAATCCTAG TTATGTGATG ACCTTGAGCC AATGACTGAA TTTCTCTGTC TCATTTTCTC 240
TTCTGTAAAA TGGGGACAAT TACAGTGAAT TCTGTGAATT CATTCATGTC CCTGACACAT 300
GGTGTGAGCT CAGTCATTAC CTTTGCGAGG GTTGCAAGGA TGTAATGAGA TGGCAGATGT 360
GAGCACAGCT CCCAGACCCG AAGGTGCTGT ATGAATGGGA GGGAGCAGTG AGTGTTATTT 420
GGGAAATATT GAAGACACAA CTTCCCTCCC ACATTTGTCT GGGGTGGAGC AACAGTTTTA 480
CTTATTTAAT GATAAGCTGG AAGATGCACC AAAGGGAGGT GAAAAACTGA AACCGCCAAC 540
CGTTTGAGCT CCAGGCTGCA CCGAAGCGGT GTGGCTGGTG CAGATGGTGA GAGCCCCAGT 600
GCCGGCCCAC TTCCTCCATG AGTGCCACAC GCCTTTCTCA AGCTAGCCGG CTTCCCAAGG 660
CTGCAGGAAG TGGGGCCAGG AACAGGCCCT CCGGCTGTGT TGGGGGAGGC CTGGGCAGGG 720
GTTGGCAGCT GCTGGGTGTG AACGGAAGTC TTGGAGGTCC TTGAAGGTCC TGGGGCCGCC 780
TGCACAGCAG CCCCTGCCCT CTCCCTGTCC AGGCCTGCCC AGGACTAGCT TGTAGCAGAC 840
TCTTCTTGTA GCCTAGGCTC TTGCCTCTTG CAGTAGTGAG CCATTGTACA AAAGACATCC 900
AGCGGAGGGA GGCAGGCTGG AGAGGAGGAC AGCCGAATCT TTTCTCAAAG GAAATGCAGT 960
TGTGGTTTTG AGACGTTCAT ATTTCACATC TGTGGTTGGC GTTTCCCAGG GTTCTCAGAG 1020
GTGAATGCAG GGTCAGCCCT GTGTCACCAA ATAAGGCTCA CAGTGACCTT AGCAACAAGC 1080
TTTGCTGCCC ATTGGCTGTC ACTGCTGCCG CCTGCCAATG CGGCCTCCTG AAGGCCAGCA 1140
CTGATGCTGA GCTGAAACTT CTGCATGTGC CAAGGTCCAG CTGCCTCTGT CAGAAATCAC 1200
CGTCCTTGGA AGCAGCCACA GATAGGTAGA GAGCTCCGGA CAAAGGTGGA CAAGGTCAGT 1260
GGGAGGACTG TCCAGGTGTC CATGTTTCAG AGTCCACCTG GCCAGCATTC CATTCTCACA 1320
TAGCACCAAA CCAGCACCTT GGTGGCCTGG TCCCAGCTTG CCAGGACAAC CCCCCATTCC 1380
ACCCTGTCAA CCTTGAACTC TATAATGGTC ATCATTTCAT AGCTCTGCTC ATTTTAGTTC 1440
CACTGGGTTC TCCCTTGTGC TTGGCACTTG ACTAAGCTCC TTCTACACAT TACATCTTTT 1500
ACCTCTCTCA ACAACCCTGT GAGCCAATTA GCCCCATTTT ACAGGTGCAG AAACTGACAC 1560
CAAAGGAAGT CAGTAATGGC CCAGGTGACT GCACCACTAG TAAGTGGGGA AGTCAGAATT 1620
TAAACCCAAT TTAAACAGAC CTAGATCCCA TGCTATTAAC CATTGCACTG TATTGACAGA 1680
CACTCAATGT CCGTGCAGCT CAGTGTCTTC ATTCTGTGAC ATGGGGATGA CAGTACCGTA 1740
CCTCACAGGG TTGGGGTGAG CATTGTGTGG AGTGACTTAT GTCCAGAAGC ACACCTTTGC 1800
ACCAGTGGCC TTGGCACCCC CAAGGCATGC TCCACAAACA GCTTGCACAT TCCTTTCTCA 1860
CAGCGTGTGC TGCTGAAACA TTGAGGTTTG TGGACCGGAC TTCTCTGTAG CCCTTGTATT 1920
TAGTTTTCAC TTCCTCTTTC TTGACCTCCT CCCACCCCCC ACCCAACTGC AAGGTAGGGA 1980
GGCTACTGAG GGGCCAGCCT GTGGATTCCA GAGGGCACAG GGCTATCTGG GATGGAGGGG 2040
ACAGGGTTCT GAAGACAGAA GGTGGGAAGG TCACACTGTA AGGGCAGACA TACCCCATTT 2100
CTTCTACCTA 2110