EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS045-55073 
Organism
Homo sapiens 
Tissue/cell
Fetal_lung 
Coordinate
chr5:131780550-131783040 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs1012793chr5131781345hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT+6.71
NFKB1MA0105.4chr5:131781775-131781788TGGGGAATCCCCT-6.82
Number of super-enhancer constituents: 37             
IDCoordinateTissue/cell
SE_00037chr5:131779157-131783687Adipose_Nuclei
SE_01257chr5:131781288-131782044Adrenal_Gland
SE_01257chr5:131782565-131783056Adrenal_Gland
SE_02141chr5:131780861-131782049Aorta
SE_04124chr5:131781320-131782082Brain_Anterior_Caudate
SE_18258chr5:131780307-131784408CD4p_CD25-_Il17-_PMAstim_Th
SE_19103chr5:131782266-131783478CD4p_CD25-_Il17p_PMAstim_Th17
SE_19972chr5:131782254-131783635CD56
SE_22284chr5:131780590-131783640CD8_primiary
SE_23079chr5:131782362-131783384Colon_Crypt_1
SE_23750chr5:131781511-131782081Colon_Crypt_2
SE_23750chr5:131782503-131783333Colon_Crypt_2
SE_25340chr5:131779182-131782135DND41
SE_25340chr5:131782161-131783524DND41
SE_25784chr5:131780866-131783705Duodenum_Smooth_Muscle
SE_26597chr5:131780491-131782132Esophagus
SE_26597chr5:131782434-131783530Esophagus
SE_30917chr5:131780689-131783539Fetal_Thymus
SE_31393chr5:131781154-131782071Gastric
SE_31393chr5:131782373-131783511Gastric
SE_39368chr5:131782618-131783324Jurkat
SE_40726chr5:131780478-131783608Left_Ventricle
SE_42103chr5:131780512-131782097Lung
SE_42103chr5:131782308-131783596Lung
SE_48659chr5:131780675-131782208Right_Atrium
SE_48659chr5:131782426-131783381Right_Atrium
SE_50051chr5:131780661-131782090Sigmoid_Colon
SE_50051chr5:131782357-131783496Sigmoid_Colon
SE_52336chr5:131780692-131782190Small_Intestine
SE_52336chr5:131782369-131783517Small_Intestine
SE_53285chr5:131780643-131782272Spleen
SE_53285chr5:131782375-131783378Spleen
SE_54554chr5:131781201-131782307Stomach_Smooth_Muscle
SE_55171chr5:131781262-131781723Thymus
SE_62219chr5:131721125-131837948Tonsil
SE_65342chr5:131781301-131782282Pancreatic_islets
SE_66244chr5:131782618-131783324Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 3             
ChromosomeStartEnd
chr5131780800131782020
chr5131782323131782964
chr5131780608131782029
Number: 1             
IDChromosomeStartEnd
GH05I132443chr5131779344131783473
Enhancer Sequence
CTATGGGGAC CAAGGTTTTA TTATGCAGAT GAGGCCTCCA GGTAGCAGGC TTCAGAGAGA 60
ATGGACTGTA AATATCTCTT ATCAGTCTTA AAGAGTCAGT AATTCCAAAA GGGAAGAGGG 120
TATAACGAGG CATGTCTGGC TCCCCCTTCC CATCATGGCC TAAACTAGTT TTTCAGGTTA 180
ACTTTGGAAT GCCCTTGGCC GAGAGGAGGG GTCTATTCAG ACAGCTGGGG AGTACCTTGG 240
AATTTTCTTT TTGGTTTACA GAACACAGGC CCAGAAATGA GAACCAGGTT TAGGTCTTGC 300
TCTCCTACTC TCCACTGTGT GACTTGGGCA AGGCATCTAA TCTTTCTAAG CCTCAGTTTT 360
CTCATTTGTA GAATGGAAAT AATGCCCTTG CTTACTTCAT AGTGTCATTC AGAGGCACAG 420
ACGATAGAGA GGCAAAATTC TTGTCTTTAA CTGCCCTGAA GCTTCATGGA GGAGTTGGAC 480
AAGTACACAC ACAATGTGCT GCATACTACA CCAGAGGTAT GTCTAGGGTG TGGTAGTAGC 540
AGTGTGGAGG TAAACTAGTT CTGCCAAAAA GAGGAGACTA CAAAGCATGG GGCGTGGTGG 600
AAGTAGCCCT CCAGGGCTTT GGACTCTAAT GTTTCTCAAA CAGTAGAGTG TTAACTGTAT 660
TAAGTTGTAT TTAGTCCCTA CAACAAACCT GTGAGATAGG TGTCATCCAT TTCACATATG 720
AGCAGCTGAG GCTCAGAAAG GATCATGCAT TGGCCTGGCC TGGTATTTAT AGAGCCCCTG 780
TTGAATGCTA AGGGGCGCAA ATCTAAGTTC CTTCCTCGTA GCTCACATTC CACAGGTGAA 840
GTCACTTGCC CAAGACGAGG CTGGAATGTC AGAGCCTGGA TTCAAACCCT CATCTGGTGG 900
CCTCCCACCT TACCCTAGAA CTCACTAGCC CTCAGGACAT CCTCTTACGG GGAGCATAGA 960
CTGTCCCTGC CAGCCCCTGT GGGGAATTTG AGGATTTAGG GAAAAGGCTG GGTCAGGGAT 1020
AGGACAGGCC CTGCTACTCC TATGGAACCT TCTGTTTCCT GAGCATTCCC TGGCAGCCCC 1080
TCCCCAAAGA GAGATTGAAG GCCTGACCGT GCCAATGTTT TCCCCAGGGA CGGAGGGCAG 1140
GAGAAGCTTC CCCAGGGGAT TTCAAGGGAG GATGGAGGTG GTCTCTATTC TGGGGTCAGA 1200
GAGTGACACC CTCTTCCTGC TGAGGTGGGG AATCCCCTTG GATTTCTCTG GGTTTATGGG 1260
AGAGGCCTAT TGTTTTCGTA CTGATCAGGC CCTCAGGGGA GGAAAACTCA AGACCTGGCA 1320
TGTCATAGGA CTAAATCAGC CTCTGGCATC TGAGTGGCTC CTTAGGCTTG GGGCTCATTC 1380
CTGCCCTCCC ATGCCCTCAG CCTCAGGCTG CCATGAGACC CATGGCACTG CCACTGGGCA 1440
GTGACATTTT GTTTTAACCC AAGGAAATAA GAGATTGGCA AACCCCCTTC TCCAAGGAAA 1500
AATATACAGG ATTGTTTATT AGAGCATTTG CTGGTAGTAA CAATCATAGG AAACAATGTA 1560
AATGGCCAAT GTTTAGGAAT TAAATAAAAT ATGGTAAAAA TCTACATATA ATGAAATACT 1620
TTTAATGCAG CCATTTAAAC TCATTATGTA GAAGAAAATT AATTTCATGA GAAGAGTGCT 1680
TTATAACAGA TTTAGTCAAA ATTCAGATCA TAAAACACAA TGTACATGAT CTCATTTTTA 1740
ACCCAAGGAA ATAAGAAAAA AAATACCTAT ATATATGCAT AGAAGAATGT CTAGAAGGAT 1800
GCATCCAAAG TTAATTGTAG TTATTTCTGG GTAGTAGAAT GACACGTTTT CTCCTGTTTT 1860
CAATATTTCC AAGTTTCCTT CAGTGAAAAT GCATGTATTT TGTAATCATG GAGAAAAAGT 1920
TCCCATGGTG TGTATTGGCG AGAGAAGAGG ATTGTTTCCT TTTGGCTTTG CACTTAGATG 1980
GCCCAAGGCC TTGGCCTTGT TCCCAGAGTG CAGATATTGT AGAAGCCACG GGGAAGGCTG 2040
GGAGCAGCAG AGGAGAGGCC AGCTTGAGGA GAATAAGCTG GGCATCGCTG TCTAGGTGTC 2100
ATCCTAAATG TCACCTCCCA GAGAGGCACC TGACCACACA GCCTGGCGAA AGGAGGTCGC 2160
TCCCACACTT ACTCTGTGTG TTTCACCCCA GCTTACTGTC TTCATAGCAC CCATCTGCAT 2220
CTGAAGTTAC CTGCCTGCAT ATCCATTTCC TTGGTGATTA TTTATCTCCT GCACAGAAGG 2280
CAAGCTCTCC AAGAGCAGAG TCCCTTGCTC ACTCTGACTT CCCATTAGGA GAAAGGACCC 2340
AAGCCAGATC TTGGTCAACA AGCAACTGAG GACTTGCTCA GCAGCCCCAA GCTATGGGCA 2400
TTTATCCTAA GGCTACACAC AGCAGTGAGA AAAAGGAAAT AACTTCATAG GAATCTAGAA 2460
ACAGGTGGAG AGCTAGCTTA TAGGACCAGA 2490