EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS082-29037 
Organism
Homo sapiens 
Tissue/cell
HCASMC 
Coordinate
chr5:131780860-131783030 
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: 1             
ChromosomeStartEnd
chr5131782323131782964
Number: 1             
IDChromosomeStartEnd
GH05I132443chr5131779344131783473
Enhancer Sequence
TCCACTGTGT GACTTGGGCA AGGCATCTAA TCTTTCTAAG CCTCAGTTTT CTCATTTGTA 60
GAATGGAAAT AATGCCCTTG CTTACTTCAT AGTGTCATTC AGAGGCACAG ACGATAGAGA 120
GGCAAAATTC TTGTCTTTAA CTGCCCTGAA GCTTCATGGA GGAGTTGGAC AAGTACACAC 180
ACAATGTGCT GCATACTACA CCAGAGGTAT GTCTAGGGTG TGGTAGTAGC AGTGTGGAGG 240
TAAACTAGTT CTGCCAAAAA GAGGAGACTA CAAAGCATGG GGCGTGGTGG AAGTAGCCCT 300
CCAGGGCTTT GGACTCTAAT GTTTCTCAAA CAGTAGAGTG TTAACTGTAT TAAGTTGTAT 360
TTAGTCCCTA CAACAAACCT GTGAGATAGG TGTCATCCAT TTCACATATG AGCAGCTGAG 420
GCTCAGAAAG GATCATGCAT TGGCCTGGCC TGGTATTTAT AGAGCCCCTG TTGAATGCTA 480
AGGGGCGCAA ATCTAAGTTC CTTCCTCGTA GCTCACATTC CACAGGTGAA GTCACTTGCC 540
CAAGACGAGG CTGGAATGTC AGAGCCTGGA TTCAAACCCT CATCTGGTGG CCTCCCACCT 600
TACCCTAGAA CTCACTAGCC CTCAGGACAT CCTCTTACGG GGAGCATAGA CTGTCCCTGC 660
CAGCCCCTGT GGGGAATTTG AGGATTTAGG GAAAAGGCTG GGTCAGGGAT AGGACAGGCC 720
CTGCTACTCC TATGGAACCT TCTGTTTCCT GAGCATTCCC TGGCAGCCCC TCCCCAAAGA 780
GAGATTGAAG GCCTGACCGT GCCAATGTTT TCCCCAGGGA CGGAGGGCAG GAGAAGCTTC 840
CCCAGGGGAT TTCAAGGGAG GATGGAGGTG GTCTCTATTC TGGGGTCAGA GAGTGACACC 900
CTCTTCCTGC TGAGGTGGGG AATCCCCTTG GATTTCTCTG GGTTTATGGG AGAGGCCTAT 960
TGTTTTCGTA CTGATCAGGC CCTCAGGGGA GGAAAACTCA AGACCTGGCA TGTCATAGGA 1020
CTAAATCAGC CTCTGGCATC TGAGTGGCTC CTTAGGCTTG GGGCTCATTC CTGCCCTCCC 1080
ATGCCCTCAG CCTCAGGCTG CCATGAGACC CATGGCACTG CCACTGGGCA GTGACATTTT 1140
GTTTTAACCC AAGGAAATAA GAGATTGGCA AACCCCCTTC TCCAAGGAAA AATATACAGG 1200
ATTGTTTATT AGAGCATTTG CTGGTAGTAA CAATCATAGG AAACAATGTA AATGGCCAAT 1260
GTTTAGGAAT TAAATAAAAT ATGGTAAAAA TCTACATATA ATGAAATACT TTTAATGCAG 1320
CCATTTAAAC TCATTATGTA GAAGAAAATT AATTTCATGA GAAGAGTGCT TTATAACAGA 1380
TTTAGTCAAA ATTCAGATCA TAAAACACAA TGTACATGAT CTCATTTTTA ACCCAAGGAA 1440
ATAAGAAAAA AAATACCTAT ATATATGCAT AGAAGAATGT CTAGAAGGAT GCATCCAAAG 1500
TTAATTGTAG TTATTTCTGG GTAGTAGAAT GACACGTTTT CTCCTGTTTT CAATATTTCC 1560
AAGTTTCCTT CAGTGAAAAT GCATGTATTT TGTAATCATG GAGAAAAAGT TCCCATGGTG 1620
TGTATTGGCG AGAGAAGAGG ATTGTTTCCT TTTGGCTTTG CACTTAGATG GCCCAAGGCC 1680
TTGGCCTTGT TCCCAGAGTG CAGATATTGT AGAAGCCACG GGGAAGGCTG GGAGCAGCAG 1740
AGGAGAGGCC AGCTTGAGGA GAATAAGCTG GGCATCGCTG TCTAGGTGTC ATCCTAAATG 1800
TCACCTCCCA GAGAGGCACC TGACCACACA GCCTGGCGAA AGGAGGTCGC TCCCACACTT 1860
ACTCTGTGTG TTTCACCCCA GCTTACTGTC TTCATAGCAC CCATCTGCAT CTGAAGTTAC 1920
CTGCCTGCAT ATCCATTTCC TTGGTGATTA TTTATCTCCT GCACAGAAGG CAAGCTCTCC 1980
AAGAGCAGAG TCCCTTGCTC ACTCTGACTT CCCATTAGGA GAAAGGACCC AAGCCAGATC 2040
TTGGTCAACA AGCAACTGAG GACTTGCTCA GCAGCCCCAA GCTATGGGCA TTTATCCTAA 2100
GGCTACACAC AGCAGTGAGA AAAAGGAAAT AACTTCATAG GAATCTAGAA ACAGGTGGAG 2160
AGCTAGCTTA 2170