EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS094-33625 
Organism
Homo sapiens 
Tissue/cell
hMADS-3 
Coordinate
chr5:131781220-131783530 
Target genes
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: 38             
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_09163chr5:131782946-131784930CD14
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: 2             
ChromosomeStartEnd
chr5131782323131782964
chr5131783026131783473
Number: 1             
IDChromosomeStartEnd
GH05I132443chr5131779344131783473
Enhancer Sequence
TTAGTCCCTA CAACAAACCT GTGAGATAGG TGTCATCCAT TTCACATATG AGCAGCTGAG 60
GCTCAGAAAG GATCATGCAT TGGCCTGGCC TGGTATTTAT AGAGCCCCTG TTGAATGCTA 120
AGGGGCGCAA ATCTAAGTTC CTTCCTCGTA GCTCACATTC CACAGGTGAA GTCACTTGCC 180
CAAGACGAGG CTGGAATGTC AGAGCCTGGA TTCAAACCCT CATCTGGTGG CCTCCCACCT 240
TACCCTAGAA CTCACTAGCC CTCAGGACAT CCTCTTACGG GGAGCATAGA CTGTCCCTGC 300
CAGCCCCTGT GGGGAATTTG AGGATTTAGG GAAAAGGCTG GGTCAGGGAT AGGACAGGCC 360
CTGCTACTCC TATGGAACCT TCTGTTTCCT GAGCATTCCC TGGCAGCCCC TCCCCAAAGA 420
GAGATTGAAG GCCTGACCGT GCCAATGTTT TCCCCAGGGA CGGAGGGCAG GAGAAGCTTC 480
CCCAGGGGAT TTCAAGGGAG GATGGAGGTG GTCTCTATTC TGGGGTCAGA GAGTGACACC 540
CTCTTCCTGC TGAGGTGGGG AATCCCCTTG GATTTCTCTG GGTTTATGGG AGAGGCCTAT 600
TGTTTTCGTA CTGATCAGGC CCTCAGGGGA GGAAAACTCA AGACCTGGCA TGTCATAGGA 660
CTAAATCAGC CTCTGGCATC TGAGTGGCTC CTTAGGCTTG GGGCTCATTC CTGCCCTCCC 720
ATGCCCTCAG CCTCAGGCTG CCATGAGACC CATGGCACTG CCACTGGGCA GTGACATTTT 780
GTTTTAACCC AAGGAAATAA GAGATTGGCA AACCCCCTTC TCCAAGGAAA AATATACAGG 840
ATTGTTTATT AGAGCATTTG CTGGTAGTAA CAATCATAGG AAACAATGTA AATGGCCAAT 900
GTTTAGGAAT TAAATAAAAT ATGGTAAAAA TCTACATATA ATGAAATACT TTTAATGCAG 960
CCATTTAAAC TCATTATGTA GAAGAAAATT AATTTCATGA GAAGAGTGCT TTATAACAGA 1020
TTTAGTCAAA ATTCAGATCA TAAAACACAA TGTACATGAT CTCATTTTTA ACCCAAGGAA 1080
ATAAGAAAAA AAATACCTAT ATATATGCAT AGAAGAATGT CTAGAAGGAT GCATCCAAAG 1140
TTAATTGTAG TTATTTCTGG GTAGTAGAAT GACACGTTTT CTCCTGTTTT CAATATTTCC 1200
AAGTTTCCTT CAGTGAAAAT GCATGTATTT TGTAATCATG GAGAAAAAGT TCCCATGGTG 1260
TGTATTGGCG AGAGAAGAGG ATTGTTTCCT TTTGGCTTTG CACTTAGATG GCCCAAGGCC 1320
TTGGCCTTGT TCCCAGAGTG CAGATATTGT AGAAGCCACG GGGAAGGCTG GGAGCAGCAG 1380
AGGAGAGGCC AGCTTGAGGA GAATAAGCTG GGCATCGCTG TCTAGGTGTC ATCCTAAATG 1440
TCACCTCCCA GAGAGGCACC TGACCACACA GCCTGGCGAA AGGAGGTCGC TCCCACACTT 1500
ACTCTGTGTG TTTCACCCCA GCTTACTGTC TTCATAGCAC CCATCTGCAT CTGAAGTTAC 1560
CTGCCTGCAT ATCCATTTCC TTGGTGATTA TTTATCTCCT GCACAGAAGG CAAGCTCTCC 1620
AAGAGCAGAG TCCCTTGCTC ACTCTGACTT CCCATTAGGA GAAAGGACCC AAGCCAGATC 1680
TTGGTCAACA AGCAACTGAG GACTTGCTCA GCAGCCCCAA GCTATGGGCA TTTATCCTAA 1740
GGCTACACAC AGCAGTGAGA AAAAGGAAAT AACTTCATAG GAATCTAGAA ACAGGTGGAG 1800
AGCTAGCTTA TAGGACCAGA CCTGGGTGGT GCTCAGCAAG CTGGAGGACC TGGCCCAGTG 1860
TTAGTAACAA CAGCGGCCAC GTACAGGTGT TGAGGAAGTA CCAGCTTTGT GTTTTCTCTT 1920
AAGGTGGAAC CAATGTAGGT TAGATCCCTC TCCCTCTGCT TCCAGCCCTC CTGCTGTCAC 1980
CAGCCAACTC CACCCCTCAG CTCCCAAATT CAGCTCCTCT CTTTAGAACC TGCTGTAGTC 2040
AGATTCTCAC TCCAACTGTT CCACTGAATC ATCCCTGACC AGGATCACCT GTGACTCCAA 2100
GATGCTAAAT CTCTGTCTTC ATATTATTAA ATAGTTGATC TATCACAGTG GACTATGCCA 2160
TCCTCCTCAG AAGTCTTTCT CCAGGTTTCC CTCCTACTGT ACTTGCTAGT CCTTTTCAGT 2220
CTCTTTTGCT GAGCTACTGA ATGGGGCTCA GCCCCTTGCA CAGCTTCCCT GGTTTTTTTT 2280
TTTTCTTTTC TTTTCTTTTC TTTTCTTTTT 2310