EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species

TagContent
EnhancerAtlas ID
HS193-20189 
Organism
Homo sapiens 
Tissue/cell
U87 
Coordinate
chr2:238612930-238614110 
TF binding sites/motifs
Number: 8             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EGR4MA0733.1chr2:238613828-238613844AAGTGGGTGGGCGTGC-6.66
ELK1MA0028.2chr2:238613279-238613289CACTTCCGGT-6.02
ELK4MA0076.2chr2:238613278-238613289CCACTTCCGGT+6.32
ERGMA0474.2chr2:238613279-238613289CACTTCCGGT-6.02
ETS1MA0098.3chr2:238613279-238613289CACTTCCGGT-6.02
FEVMA0156.2chr2:238613279-238613289CACTTCCGGT-6.02
FLI1MA0475.2chr2:238613279-238613289CACTTCCGGT-6.02
GabpaMA0062.2chr2:238613277-238613288GCCACTTCCGG-6.62
Number of super-enhancer constituents: 36             
IDCoordinateTissue/cell
SE_00318chr2:238608341-238613202Adipose_Nuclei
SE_01566chr2:238612977-238617649Aorta
SE_02327chr2:238610486-238613462Astrocytes
SE_09199chr2:238608075-238617357CD14
SE_11030chr2:238594416-238614117CD20
SE_14422chr2:238613101-238614392CD4_Memory_Primary_7pool
SE_17823chr2:238594491-238617199CD4p_CD25-_CD45ROp_Memory
SE_18373chr2:238600747-238613962CD4p_CD25-_Il17-_PMAstim_Th
SE_19179chr2:238608152-238616656CD4p_CD25-_Il17p_PMAstim_Th17
SE_22424chr2:238612926-238614152CD8_primiary
SE_23331chr2:238613197-238614210Colon_Crypt_1
SE_23963chr2:238613569-238613901Colon_Crypt_2
SE_24998chr2:238613420-238614115Colon_Crypt_3
SE_25815chr2:238608299-238618181Duodenum_Smooth_Muscle
SE_26722chr2:238612937-238613948Esophagus
SE_28399chr2:238612936-238614838Fetal_Intestine
SE_29463chr2:238612762-238614953Fetal_Intestine_Large
SE_36086chr2:238610778-238613929HMEC
SE_36919chr2:238608262-238615293HSMMtube
SE_38133chr2:238608238-238614216HUVEC
SE_40633chr2:238608186-238614216Left_Ventricle
SE_42111chr2:238608226-238618523Lung
SE_43921chr2:238608281-238613700MM1S
SE_45786chr2:238608313-238614636Osteoblasts
SE_48071chr2:238612981-238614148Psoas_Muscle
SE_48757chr2:238612977-238613972Right_Atrium
SE_51094chr2:238608086-238615331Skeletal_Muscle
SE_51777chr2:238610510-238614092Skeletal_Muscle_Myoblast
SE_52590chr2:238612978-238614148Small_Intestine
SE_54582chr2:238608047-238614343Stomach_Smooth_Muscle
SE_58523chr2:238563966-238621920Ly1
SE_59868chr2:238570692-238624050Ly4
SE_62022chr2:238577134-238613107Toledo
SE_63565chr2:238610411-238614143HSMM
SE_65656chr2:238607949-238613154Pancreatic_islets
SE_67420chr2:238608281-238613700MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2238613023238613083
Number: 1             
IDChromosomeStartEnd
GH02I237699chr2238608260238614656
Enhancer Sequence
GATTACAGGT GCCCACCACC ACGCCCAGCT AATTTTTTGT ATTTTTAGTA GAGACAGGGT 60
TTCACCATGT TGGCCAGGCT GGTCTCAATC TCCCGACCTC AGGTGATCCG CCCACCTCAG 120
TCCCCCAAAG TGCTGGGATT ACAGGTGTGA ACCACCGCGC CTGGCCAACT CTACGGATTT 180
TCTCTCAGGC ATCTTAAGCA AGTGGCAAGA GTTATTCTGT GGCTAAGTGT GTAGTTTTGT 240
GTTCGTGAAG ATGGTCATGC ATAGGTTTTG TGCCAGTTTA AATGCTGGCT CATATATTTG 300
TTGGTGTTGA GTTAGGCAGA TTCCAAGAAT TGCCTGTAAG CTAAGTTGCC ACTTCCGGTA 360
TTGCCAGCAC TTTGTTTTCC ACATATGAGT CATGTGAGGA TCGTAAGGGG GGTAGATGTT 420
CTAGAAGGCA GGGGCTGCAA GGATTTGGAA TTGTATTCAG TGACAAATGG ACTTCTTTCT 480
GAATTCTAAT GTAAGGTGGA GATCGCCATA GTTGACCTGT CTTGGAGGTG GGCTTGCGTG 540
TGTCCCCATG AGGAATTGAT GCCCTAACAT GATTCATCCA TGGGGTTCCT TTATCAGCCC 600
AAGCCCATGT GCCTCCCAGC AAAGGTCATT GTTTTTTAGT CTTTAAATGT CATTATCCCC 660
AAGTGAGGGA CAGGGTAAAC CTGTTAGGCT GAAGGTGGGC CATGATGGGA ACCTTTTCCT 720
GGGTGGAGGG CAGACCCCCG AGAGCAGCGG GGTCTGACAG GGCATTGTTT TGGAGGCCTG 780
CAAGTCTGGA GCAGGTGCAA TACTGCACGC TCAGGCAGGC GAGCTCTGCA AGGACCTTTG 840
GCCAGACCCG AGCAGAGCTA AGCTGGAATA GGGTGGGGTA CTGAGCAGGC AGGCGGGGAA 900
GTGGGTGGGC GTGCAGGTGC CTGGGACCCC CCTCAGCTCA CAGAGATACT CGCCCTGTGA 960
GAGCAGGAGT CACCTCAGAC CTCCTCTCCT TCTGTTATCT GCTAGTGTGT AATAAATATC 1020
CACAATTCAG CGGCTTAGAA TAACACACAG TTATGATCTC ACAGTTTCTG TGGTCAGGAG 1080
TCTGGGCACA TTGGCCAAGC GCAGTGGCTC ATGCTGGTAA TCCCAGCACT TTGGGAGGCT 1140
GAGGCAGGTG AGTGGCATGA ACCCAGGAGT TCGAGACCAG 1180