EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS162-11020 
Organism
Homo sapiens 
Tissue/cell
Plasma_cell_myeloma 
Coordinate
chr9:134603060-134604940 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Gata1MA0035.3chr9:134604319-134604330ACAGATAAGGA-6.14
IRF1MA0050.2chr9:134604037-134604058AGAGAGAAAGAGAAAGAACAA-6.64
LMX1BMA0703.2chr9:134603731-134603742GATTTAATTAA+6.02
RREB1MA0073.1chr9:134604729-134604749GTTGGGTGGGTGGGTGGGTG-6.37
Number of super-enhancer constituents: 40             
IDCoordinateTissue/cell
SE_00686chr9:134602683-134604709Adipose_Nuclei
SE_04525chr9:134602365-134603378Brain_Anterior_Caudate
SE_04525chr9:134603515-134604908Brain_Anterior_Caudate
SE_09150chr9:134602020-134613269CD14
SE_10404chr9:134599070-134613095CD19_Primary
SE_10884chr9:134591844-134615384CD20
SE_12120chr9:134602204-134605810CD3
SE_14804chr9:134601937-134605983CD4_Memory_Primary_7pool
SE_16701chr9:134601791-134611990CD4_Naive_Primary_8pool
SE_17150chr9:134602259-134605741CD4p_CD225int_CD127p_Tmem
SE_17952chr9:134601452-134615329CD4p_CD25-_CD45ROp_Memory
SE_18769chr9:134601534-134615309CD4p_CD25-_Il17-_PMAstim_Th
SE_19472chr9:134602036-134615436CD4p_CD25-_Il17p_PMAstim_Th17
SE_20363chr9:134601294-134613216CD56
SE_22914chr9:134601848-134613223CD8_primiary
SE_27117chr9:134602474-134605235Esophagus
SE_30786chr9:134603605-134604770Fetal_Muscle
SE_31710chr9:134604237-134605201Gastric
SE_32578chr9:134599803-134613266GM12878
SE_33628chr9:134601311-134605438H2171
SE_36750chr9:134601897-134605432HMEC
SE_36915chr9:134602036-134616473HSMMtube
SE_38234chr9:134602233-134605128HUVEC
SE_40722chr9:134604237-134605417Left_Ventricle
SE_42566chr9:134602550-134603408Lung
SE_42566chr9:134603476-134605411Lung
SE_44033chr9:134602118-134608169MM1S
SE_50405chr9:134601862-134605454Sigmoid_Colon
SE_52037chr9:134602527-134603740Skeletal_Muscle_Myoblast
SE_52732chr9:134602045-134605560Small_Intestine
SE_54202chr9:134601963-134613163Spleen
SE_58352chr9:134520171-134620333Ly1
SE_58881chr9:134579557-134620273Ly3
SE_60383chr9:134599961-134620084Ly4
SE_60991chr9:134494570-134620113HBL1
SE_61989chr9:134594251-134616125Toledo
SE_62218chr9:134495530-134621458Tonsil
SE_63796chr9:134602444-134603555HSMM
SE_64992chr9:134602127-134605438NHEK
SE_66603chr9:134602516-134605411Jurkat
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr9134603973134604163
Enhancer Sequence
CCCTGCAGCA CAGGCAGTCC CTAGCCCGAG TCCCTGTAAT CCAGGTCCCT AGCCCAATTC 60
TTACTTGTCA AATATAAAAG CTTCATTCTA CAACCTTGCA TATTTAGGGT AATTAATAGA 120
GAAAGCTCCT CATGAACAGA AAAAAAACAA GGACAGATCA TGCAGAAAAG CATGCTTTTG 180
ATCTATGCCT TTGGTCTTCT GATGAGCTCA GAGAATTAAT ATTTGCAAGG CACTCTTGAC 240
AAGCTGAGGC AGAAGCACAA ATTAGTGTGG TTATGCTAAT TGAGAGGTTC TGTAGCTCCA 300
GGACCAAATG ATTACAGAAA GTGAAAAGGG TTGACTGGGC TTTGGTCTCT CTGCAAATAG 360
CACTGTGCTT CATGCTAGCT GCACTGACAA ATTTGCAAGG AGACTACACA CATTTACTTT 420
CACATACCCG AAATTCCCAG TGGAGCAGGG GTTAAGGAAG ACTCAGAACA CCAAAACAGC 480
ATTTCTGAAT TTATCTTTAC TGTGAAAGTT AATCAAGAAA GAAAAATAAA GGGTATGAAA 540
TCCCCCTTCT TGCAGTGCTC AATGCAACTT GTAAGTTACT TTGTACACGA GGACCTTGAA 600
TGTCTTGTGG TTTTTAACTG TCACAAATGC AACACTCTGT GATCATTTCA CCTCCAGAGC 660
TGAACGAAGA TGATTTAATT AATCCCCGAA AGTCACCCCG CAAGGAGAAA CTGGGGAGGT 720
GTCCCTTGAG ACAGGGCAAA AAATATACCT GTTGGTGTAT CAGCCCTGCT GTGGCTCTGA 780
CATATACCAC AGCCTGCAAG CACAGGCCCA TTCCTTCCAG ACAGACTCAA ATTAAAATCA 840
GGGCCTCCTG GTCTGCCTGC ATGCACTGGG ATATGTGTAG CTGAAATGAA TTGCCCTCTA 900
CTCTTCCTAC GAGTGATCAC TTCAAAAGTT TATTACTTAA TTGTAAAAAC CTACTCCCTG 960
GACTTCAGCT TTCTTAGAGA GAGAAAGAGA AAGAACAAAC CAGCCTAAAA GGAAATACCT 1020
CAATAGTCAG GGACCTCCCC TTCTCTGTGA GTGCTGAGGT TTGAATTTTA GTTACCAGAT 1080
TACCATTTTT AAAGAAATGG TCACTTTAGA GTAGAAGGCG ACCTGAAGTA AGAACAAAAG 1140
CTAAGATTTA TCGAGCACTT CTTATGTGTC CAGACTCTGA TTAAATGCTT ATGTACATCA 1200
TCTCGTTTAA TTCTCCCTCA ATACCATAAG GTAGGTACTG TTAGGATTTT CCCCATTTTA 1260
CAGATAAGGA AAAACTGAGA GTTAGACAAG ACAGAGTGAC ATGCCCAAGA TCCCACAACA 1320
ATGACACAGG AGGGCTGGTA TCTAAAGCCA CAGCTAGAGG ACCTGAAGCA CATGCTCTCA 1380
GACACTGTTC TGTACTGGCT CACTGCACAG ATGGAAAGAC AGGGTTGGGG AGGGGCACTG 1440
ATCCAGTGCA TCAGTGCAGG CCCAGGGGCC ATGAGGCAGG TCTCCCACCT CTCAGCTCAG 1500
GCTCATGCTG CCTCTAACAC GGATGAGGGT GTGAGAGCCA AGATCAAAAG TCTCCTGTAC 1560
ACAACGCAGG TGGTGGCTGA CTGTCAGTTC CCCAAGGGCA CTGACGCCTC AGCCCTCTCA 1620
GTACCCTCTC CTCCCCTGGC AGGCTGCTTG ACACTCAGTG ACAGCCAGTG TTGGGTGGGT 1680
GGGTGGGTGG AACTACTTTA ACTCGTAAGG GCCACTTCCT ACCGTTGTGC CATCTGTGAA 1740
AGGTTTCTCC AAAGCAGATT CTCATGCAAT ATTTTCAGCA AATGTACTTT TTAAGCCACT 1800
TCAATAATGG AGAAACCAGG GGCTTCTTCA TAAATCTGTA GGCAGATGTG GTGCCACCTT 1860
AACAGTCCTA CAGAGAGGCT 1880