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

TagContent
EnhancerAtlas ID
HS048-22428 
Organism
Homo sapiens 
Tissue/cell
Fetal_small_intestine 
Coordinate
chr2:238612980-238615180 
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: 42             
IDCoordinateTissue/cell
SE_00318chr2:238608341-238613202Adipose_Nuclei
SE_00318chr2:238614544-238615875Adipose_Nuclei
SE_01566chr2:238612977-238617649Aorta
SE_02327chr2:238610486-238613462Astrocytes
SE_09199chr2:238608075-238617357CD14
SE_11030chr2:238594416-238614117CD20
SE_11030chr2:238614296-238617234CD20
SE_13435chr2:238614109-238614995CD34_Primary_RO01536
SE_14422chr2:238613101-238614392CD4_Memory_Primary_7pool
SE_17380chr2:238614307-238617265CD4p_CD25-_CD45RAp_Naive
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_40633chr2:238614535-238615385Left_Ventricle
SE_42111chr2:238608226-238618523Lung
SE_43921chr2:238608281-238613700MM1S
SE_45786chr2:238608313-238614636Osteoblasts
SE_48071chr2:238612981-238614148Psoas_Muscle
SE_48071chr2:238614369-238617012Psoas_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_54582chr2:238614727-238618024Stomach_Smooth_Muscle
SE_58523chr2:238563966-238621920Ly1
SE_59868chr2:238570692-238624050Ly4
SE_63565chr2:238610411-238614143HSMM
SE_65656chr2:238614594-238615419Pancreatic_islets
SE_67420chr2:238608281-238613700MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr2238613023238613083
Number: 2             
IDChromosomeStartEnd
GH02I237699chr2238608260238614656
GH02I237706chr2238615027238615313
Enhancer Sequence
GAGACAGGGT TTCACCATGT TGGCCAGGCT GGTCTCAATC TCCCGACCTC AGGTGATCCG 60
CCCACCTCAG TCCCCCAAAG TGCTGGGATT ACAGGTGTGA ACCACCGCGC CTGGCCAACT 120
CTACGGATTT TCTCTCAGGC ATCTTAAGCA AGTGGCAAGA GTTATTCTGT GGCTAAGTGT 180
GTAGTTTTGT GTTCGTGAAG ATGGTCATGC ATAGGTTTTG TGCCAGTTTA AATGCTGGCT 240
CATATATTTG TTGGTGTTGA GTTAGGCAGA TTCCAAGAAT TGCCTGTAAG CTAAGTTGCC 300
ACTTCCGGTA TTGCCAGCAC TTTGTTTTCC ACATATGAGT CATGTGAGGA TCGTAAGGGG 360
GGTAGATGTT CTAGAAGGCA GGGGCTGCAA GGATTTGGAA TTGTATTCAG TGACAAATGG 420
ACTTCTTTCT GAATTCTAAT GTAAGGTGGA GATCGCCATA GTTGACCTGT CTTGGAGGTG 480
GGCTTGCGTG TGTCCCCATG AGGAATTGAT GCCCTAACAT GATTCATCCA TGGGGTTCCT 540
TTATCAGCCC AAGCCCATGT GCCTCCCAGC AAAGGTCATT GTTTTTTAGT CTTTAAATGT 600
CATTATCCCC AAGTGAGGGA CAGGGTAAAC CTGTTAGGCT GAAGGTGGGC CATGATGGGA 660
ACCTTTTCCT GGGTGGAGGG CAGACCCCCG AGAGCAGCGG GGTCTGACAG GGCATTGTTT 720
TGGAGGCCTG CAAGTCTGGA GCAGGTGCAA TACTGCACGC TCAGGCAGGC GAGCTCTGCA 780
AGGACCTTTG GCCAGACCCG AGCAGAGCTA AGCTGGAATA GGGTGGGGTA CTGAGCAGGC 840
AGGCGGGGAA GTGGGTGGGC GTGCAGGTGC CTGGGACCCC CCTCAGCTCA CAGAGATACT 900
CGCCCTGTGA GAGCAGGAGT CACCTCAGAC CTCCTCTCCT TCTGTTATCT GCTAGTGTGT 960
AATAAATATC CACAATTCAG CGGCTTAGAA TAACACACAG TTATGATCTC ACAGTTTCTG 1020
TGGTCAGGAG TCTGGGCACA TTGGCCAAGC GCAGTGGCTC ATGCTGGTAA TCCCAGCACT 1080
TTGGGAGGCT GAGGCAGGTG AGTGGCATGA ACCCAGGAGT TCGAGACCAG CCTGGGCAAC 1140
ACGGCAAAAC CCTGTCTGTA CAAAAAAATA CAAAAATTAG CTGGGTGTGG TGGCACCTGC 1200
CCTGTAGTGC CAGCTACTTG GGAGGCCGAG GTGGGAGAAT CACTTGAACC TGGGAGGCAG 1260
AGGTTACAAT GAGCTGTGAT CACGCCACTG CACTCCAGCC TGGGCGACAG AGGGAGACCC 1320
TGTCTCCAAA AAAAAAAAAA GAGCCTGGAC TCAGCCTCTC TGGGTCCTGT GCTCAGGTCT 1380
CACAAGGCTG CAACCAAGGT GTCGGCCAGT CTGGGGTCTT TCTGGAGTTC AGGCCCCTCT 1440
TCTGAGCCAC GTGTTTGTTG GAAGAATTCA GTTCCTTGTG GTTGTAGGAC TGTGGTCACT 1500
GTTCCTGCTG GCGTCAGTCA GCCAGGGGCT GCTCTCAGCT CATCGAGGCC CCCTCCCACT 1560
GGGCAGCTTG CTTTCTCAAA GCCAGCAAGG ACACTGACTT CTAGACCCTC TTTTAAAGGG 1620
CTTGCCTGAT TAGGGCAGGC CCATAGGATA ATCTGTCTTT TGAGCAAGGC AGTCAACTGA 1680
CGAAGGATTT TAATTATTTT TTTAATACTT TTTGCCATGT AATACAGCCT AATTACAGTG 1740
GTGTCATCCA TTATGTCCAT GGTCCCACGC ACTCAGTGGG AGAGGGGTAT GCAGGGCAGG 1800
TACACTAGTG GTGGGAGTCT TGGGGACCAA CCCAGAATTC CACGTTCCCA CACAGTGGGA 1860
GAGGGGTATG CAGGGCGTGT ACACCAGAGT CTTGGGGACC AACCCAGAAT TTGGCCGACT 1920
GCAGTTGTCT CTCCCTCTGT TCCCTTCTGG TGGCCCTTCT TTCCCCCAAC CCTTTCCTCT 1980
TTCTTACATC TCACCCCTCT GCTCCTCTTC TTCTTCTTGC ATGGCCTCCC TTCTCTTTTC 2040
CCGGCCCCTC CTCTCTGTTC CTCTGCCCCC CAACCCCCAA GCTGGTGGGC TATGGCTGCT 2100
ATGAAACCTC GTACCTGCTC TGTACTGGCT TAGAAACTGA GCCAATGGCA CAGAGCCACC 2160
TGCCTTACCA GGAAGGGCTG CACTTGGCGT GGCCTTGGTC 2200