EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS182-20117 
Organism
Homo sapiens 
Tissue/cell
Spleen 
Coordinate
chr7:102055470-102058490 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12534945chr7102058179hg19
TF binding sites/motifs
Number: 6             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ELF3MA0640.1chr7:102058371-102058384TTACTTCCTGGTA-6.17
ELF5MA0136.2chr7:102058372-102058383TACTTCCTGGT-6.02
EWSR1-FLI1MA0149.1chr7:102058361-102058379CTTGGCTTCCTTACTTCC-6.44
Foxd3MA0041.1chr7:102057305-102057317GTTTGTTTGTTT+6.32
KLF4MA0039.3chr7:102057279-102057290CCACACCCTGC+6.62
Nkx2-5(var.2)MA0503.1chr7:102055555-102055566AGCCACTCAAG+6.62
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_10269chr7:102055222-102058356CD19_Primary
SE_11022chr7:102052786-102078230CD20
SE_12084chr7:102055916-102057262CD3
SE_12084chr7:102057472-102058277CD3
SE_13111chr7:102055896-102056741CD34_Primary_RO01480
SE_13774chr7:102055854-102057039CD34_Primary_RO01536
SE_16785chr7:102055545-102057464CD4_Naive_Primary_8pool
SE_17129chr7:102056040-102057064CD4p_CD225int_CD127p_Tmem
SE_17129chr7:102057707-102058220CD4p_CD225int_CD127p_Tmem
SE_17654chr7:102055359-102059666CD4p_CD25-_CD45RAp_Naive
SE_18074chr7:102055362-102059776CD4p_CD25-_CD45ROp_Memory
SE_19907chr7:102055909-102057137CD4p_CD25-_Il17p_PMAstim_Th17
SE_20233chr7:102055105-102058612CD56
SE_22677chr7:102054526-102059670CD8_primiary
SE_31146chr7:102055874-102057244Fetal_Thymus
SE_32635chr7:102055610-102057363GM12878
SE_50775chr7:102055369-102057424Sigmoid_Colon
SE_53584chr7:102055857-102057439Spleen
SE_55241chr7:102055909-102056998Thymus
SE_58603chr7:102040407-102092313Ly1
SE_59253chr7:102055636-102092627Ly3
SE_60339chr7:102055866-102075560Ly4
SE_60478chr7:102022497-102092339DHL6
SE_62031chr7:102047957-102092277Toledo
SE_62443chr7:102048336-102086597Tonsil
SE_66677chr7:102055970-102056942Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr7102056938102057102
chr7102057614102057973
Number: 1             
IDChromosomeStartEnd
GH07I102414chr7102055205102059635
Enhancer Sequence
TGACAGTGTA TGTAACAGGG TACACTCTCA CCATATCCTC AACATTTTAC TCTTCCTCCA 60
CATGGGTAAG AATGGGGCAC ATGAGAGCCA CTCAAGGTCT TACTGGGGAT TGAGTAAAAA 120
GCCTTACAGA AATACAGTGC AGACCTGCAA GACTGTGGAG GCAGTCCCAC TCTCTTGCCA 180
TTCCACCCCC CACGCACCCA CCTGTGTACA GCCTCCAAAG CTCTGTTTTT TGAAATGGAG 240
TCTTGCTCCA TCACTCATGT TGGAGTGCAG TGGCGCCAGC TCAGCTCACT GCAACCTCCG 300
CCTCCCAGGT TCAAGAGATT CTCCCACTTC AGCCTCCCAA GTAGCTGGGA TTACAGGCGA 360
CTGCCACCAC ACCAGCTAAT TTTTGTATTT TTAGTAGAGA TGGGGTTTCG CCATGTTGGC 420
CAGGCTGGTC TTGAACTCCT GATTTCAGGT GATTCACCCG CGTTGGCCTC CCAAAGCGCT 480
GGGATTACAG GCGTGAGCCA CCGCACCCAG CCCCAAAGCT ATTTTATAAA ATGTACATTG 540
GATTGTCAGT CATTCTTCTG CCTTTACAAC AATACCCAAG ATCACGGAAT GCTTCTTACG 600
TACCCCTAGT TCTAAATGCT TTGCTTGTAT TAACTAACAA TCCTTACAGC AGCCCTGTGA 660
GGTTAGTCAG TGGTGCTGTT ATCCCCATTT TACTAATGAC AGACCTTAGG CACCATGCGG 720
TGATGGCACC CACAAAGCTG CAGAGGATGT GGGCAGCAGG CCAGGGTGTG ATCCCAGGCA 780
CCCACACCCG CCCATGAGGC GATGCTGCGT GAAACCCTGT CAGCAGCCCC AGTGTTCCTG 840
GCCCTCACGG TCTGGCCCCT TCCGGTCTCC ACCATGCTGG TCTGTTCACT CCCTTCCACA 900
TGCCCCCAGC TCTCTGTCCC TCAGCCTCGC TGCATGTGCT TAGGCTGCCT GTACTCTGTT 960
CACGCCGCCT GACTTCTCAT CTGACTGGAG AAGCTCTCTT CACCTTCAGC TTCCTCTTAC 1020
AATGCTTTCT GTTTGTGTAA AGCCTCTCCT CACCTTCCTC CGGCCCCCGG CCCTAGAAGT 1080
CGCCTTTCCT GCCAGCCTGC CCCATGGGGT TGTGTGTGCC CTTGGCTGCA GGCCCTGCCA 1140
GATCAGATAA GGTGCTTGTC CATTCAGCTA TGTCAGTTCC ATCTTTTTCA AAATAAGCCT 1200
CATTTTAGAA TGACTTTAGA TTCACAGAAA GATTGCAAAG ATAGTACAGA GCGTTCTCAT 1260
ATATCCAGTC TCCCCATTGT TTAACTTCCT AAATTAACCT GGTACATTGG TCACAGTGTG 1320
TGAACCCACA TCGATACACT TGTTAGCTGA AGTCCATACA TTATTCCAGC TGCCTTAGTT 1380
TTTACCTGCT GCCCTTTTCT TGCTCCAGAA TCCAATCCAG GGCACCGCGT CACATTGTGT 1440
TATTACGCAT TCTTCGGCTC CTGTTGGCTG TGACAAGTTT CTCAGACTTT CTGTGGGTCC 1500
AGTACTCTAT AAAATGGCCC TCAGTTGGGA TTGGTCTGAT TTTCTCATGA TTTGACTGGG 1560
GTAGTTTGTT TTGGGGATGA GGACCACAGA GGGAAAGCAC CCTTCTCACC ACACATCAGG 1620
GCATTGTACT GCCAACGTGG CCATCAGGTT TTGTGGGGTG TTTTTTTTTT TTTGGAGACA 1680
GGGTCTCTCT CTGTTGCCCA GGCTGGAGTA CAGTGGCACC ATCTCACCTC ACTGCAGCCT 1740
CGAACTTCTG GGCTCAGGTG ATCCTCCTTC CTCAGCCTCC TGAGTAGCTG CAACTACAGA 1800
TGCGCACCTC CACACCCTGC TAATTTTGGT GTTTTGTTTG TTTGTTTGTT GAGATGGAGT 1860
CTCGCTTTGT CGCCCAGGCT GGAGTGTGGT GGCGCGATCT TGGCTCACTG CAACCTCCGC 1920
CTCTTGGGTT CATGCCATTC TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TACAGGCACC 1980
CACCACCACT CCCGGCTAAT TTTTTGTATT TTTAGTAGAG ACGGGGTTTC ACTGTGTTAG 2040
CCAGGGTGGT CTCGATCTCC TGACCTCGTG ATCCACCCGC CTCAGCCTCC CAAAGTCCTG 2100
GGATTACATG TGTGAGCCAC CACACCTGGC TAATTTTGGT ATTTTTTCTG GAGATGGGGT 2160
CTCATTATGT TGCCCAGGCT GGTGCCATCA CTGTTGATGT TTACCTTGAT CACATGGCTG 2220
AGGTAGTGTG GTCAGGTTTC TCCCCCATAT GTTTACTCTC TTTTCCCCTT CCTGTACGTT 2280
ACTCTGTAGA AGAAAGTCGT TGTGTGCAGC CCACACATAG GGAGTGTGGG GCTGTGTTCC 2340
TCCTCCCTGA CAGTGGAGAA TCTACATGCG TCATTGAAGT CATTCTGCAT GCTAGGGTTA 2400
TTTCTTCTTT CCATGTATTT ATCATTATTT AATCATTTCC ATCTATCAGT ATGAGCTTGT 2460
GGGTATTCAT TTTGTACTTG ATAGTCCATT ATTACTGTAT TTGTTTTACT ACTCATAGTA 2520
TTCCCAGCTT TGGCCATTGG GAGCTCTTTC AGTTGGCTCC TGTGTTCCCT TGACAAAGTC 2580
CCATCATTGT GGGTACCTTT TTTTTTTTTT TTTTTTTTTG AGACAGGGTC TCTTACCTAG 2640
GCTGGAGTGC AGTGGCACCA TCATAGCTCA CTGCATCCTC AAACTCCGGG CTCAAACAAT 2700
CCTCTCGCCT CAGCTTCCTG AGTAGCTGGG CCCACAGGCA TGCACCACCA TGCCCGGCTC 2760
AGTTTTAAAA TTTTTTTGTA GAGACAAGGG TCTCGCTATA TGGCCCAGGC TGGTCTCAAA 2820
CTCCTGGGCT CAAGCAGTCC CCCTGCCTCA GCCTCCCAAA AGTGCTGGAA TTACAGGCAT 2880
GAACCACCAC ACTTGGCTTC CTTACTTCCT GGTACTATAG GATATTCCAG ACTCGTGTCT 2940
TGTGTTTCCT GCCCTGGACC TGGGATCAGC CATTTGTCCA AGAAGTCCTG GCTGCTGCTT 3000
TCTTCTTCTT CTTCTTCTTC 3020