EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS060-30321 
Organism
Homo sapiens 
Tissue/cell
GM12891 
Coordinate
chr6:111910020-111912460 
TF binding sites/motifs
Number: 1             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
SOX10MA0442.2chr6:111912036-111912047TGCTTTGTTTT-6.02
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00043chr6:111905012-111917090Adipose_Nuclei
SE_01477chr6:111910673-111911134Adrenal_Gland
SE_01477chr6:111911334-111913434Adrenal_Gland
SE_01892chr6:111910292-111913394Aorta
SE_02609chr6:111910127-111911825Astrocytes
SE_02609chr6:111911848-111913962Astrocytes
SE_24555chr6:111910660-111911012Colon_Crypt_2
SE_24555chr6:111912196-111912740Colon_Crypt_2
SE_25836chr6:111908800-111915284Duodenum_Smooth_Muscle
SE_26930chr6:111910177-111915191Esophagus
SE_28180chr6:111910460-111911278Fetal_Intestine
SE_28180chr6:111911629-111913739Fetal_Intestine
SE_29422chr6:111910287-111911511Fetal_Intestine_Large
SE_29422chr6:111911623-111915197Fetal_Intestine_Large
SE_31696chr6:111910285-111911137Gastric
SE_31696chr6:111911351-111913438Gastric
SE_33474chr6:111910290-111915988H2171
SE_36399chr6:111909247-111914904HMEC
SE_36956chr6:111908817-111916894HSMMtube
SE_38953chr6:111910082-111915170IMR90
SE_41014chr6:111910426-111911290Left_Ventricle
SE_41014chr6:111911970-111913660Left_Ventricle
SE_42404chr6:111910215-111911077Lung
SE_42404chr6:111911171-111913478Lung
SE_44157chr6:111908814-111915968NHDF-Ad
SE_44783chr6:111910076-111915214NHLF
SE_45702chr6:111908728-111916180Osteoblasts
SE_47224chr6:111907764-111917003Panc1
SE_48418chr6:111910133-111913940Psoas_Muscle
SE_49187chr6:111911244-111913429Right_Atrium
SE_50264chr6:111910257-111911154Sigmoid_Colon
SE_50264chr6:111911360-111915118Sigmoid_Colon
SE_51251chr6:111909320-111914248Skeletal_Muscle
SE_52070chr6:111909440-111915027Skeletal_Muscle_Myoblast
SE_52559chr6:111910287-111911113Small_Intestine
SE_52559chr6:111911237-111915118Small_Intestine
SE_54880chr6:111910427-111915136Stomach_Smooth_Muscle
SE_55947chr6:111908993-111914469u87
SE_63870chr6:111909299-111915041HSMM
SE_64317chr6:111908912-111915049NHEK
SE_67791chr6:111908993-111914469u87
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr6111910421111910993
Number: 1             
IDChromosomeStartEnd
GH06I111587chr6111909054111916685
Enhancer Sequence
TGCGTCTGAT GAAATACAAT GAAGCAGTTT TAAATGATTC TGGAATAAGT ACTCAATGTC 60
ACTGAAAACT ATTTTAATTT TAGATTAAAA ATATATGCAA AGAAAAAAAC ACTGAAAATT 120
GATATGTCAA AACCCTAATA AGGAATTCTA TTTGGGTGGC AGAAATATGA AAACTTTTTC 180
TTTTCTTTTT TGAACTTCTG GGCATATTTT AATTTTGGGA GTGACCAAAT ATTATAATGA 240
TCAGAAAAAT TATCTTTTTT TTTTTTTTTT TTGAGATGGA GTCTCACTGT GTCATCGCCC 300
AGGTGCAGTC TCGGCTCACT GTAACCTCTG CCTCCCAGGT TCAGGCAATT CTTGTGCCTC 360
AGTCTCCCGA GTAGCTGGGA TTACAGGCGC CCGCCACAAC AACTGGCTAA TTCTTTTTGT 420
ATTTTTAGCA GAGACAGTGT TTCACCATGT TGGCCAGGCT AGTCTCAAAC TTCTGATCTC 480
AAGTGATCCA CCCACCTTGG CCTCCCAAAG TGCTGGGATT ACAAAGTGGG GTGAGCCACC 540
GTGCCTGGTG AAAACTTACC TTTAAATACA GATAACAGAA TGTTAAAAAG TAGTTTATGG 600
TATTATTCTC ACAAATTACT CCTTTTAAAC CTGGCAATCA CTGAGAAATA CAGCCTTGAC 660
CTTGCCAACA TTCAGTTCTC AGTGATTCAT ACTTAAGGGA ATCCACCACC ACACCCACCC 720
TATGACTGGG CGCTTAGAGC AGGGGTGGCA TCCATGCACT CCCACTCTGT TGACTTCCCA 780
GCATTTATAC ACCACGTCCC AGTTTTAGGC ATCAGAGGCT CTTTCTCCCG CTCCAGCCCA 840
AGGCCCCATT CTCCTTACAC CCTCCTGCTT CCCCAGCCCC TGCCCTCATT CCTGATCTCA 900
CACTCATTCT TACCTATTTC TTCCAAGCAT CTTCTAAGTT ACATTTCTCT ATCTCCTCTT 960
TGTTTTTTTC TTTTTTGAGT TATGAATTAC TGTGTTGCTC TCTTCACTTT AGGAAGCTTT 1020
ATACTTAGTA TACATGTACT AATATGTAAA TTATGGTTGA TTACAGCATT TGTAATTATT 1080
TCTATAATTT ATTTTAAAGC TGCGCATCAG GCCTTTGGTC AGGCACTTCT TACACTCTGA 1140
ACTACTTTCT GTCCAGTGTT TATTTGCTAA GAAAAATATC AGGCCTCACA GCCCTGTGTT 1200
TCATCTGTAA AGCCCTTTTG TTATTTTCCA GTGGCCTCAG CGGAGATTTA ACATCAAGAA 1260
TGGTAGTAGG AAAAAAAAAA TGGTGATAGA ACCTTTTATC TCAACCTAAG ACTTATCACT 1320
TTCAGAGATG CTTCCTGCAC TGATACATAT TATTATTTCG GAAGTAGTTT ATTGAGAGTC 1380
TAGTATGTGC CAGACACTGT GCTTAAATCC TGGGGAATTA TGAATTGAAA GTACACGTTT 1440
GCATTTGCAG ATGCATAAAA ACTTGCAGTC TAGAAGGAGA GGAGACACGT ACATAATTAG 1500
ATGCCATGCT GGTGTTAGGT GTCCCAACAG GGCCAGAGCA GGAGGGAGAC AGAGGCCCTG 1560
AAGGAGAACG TGATCTGGGG AGGTTTCCAG AGGGACACTT GAGCTAAGTC TCAAAAAATG 1620
TGTATGATGG TGGTTGCATA ACTCTGTAAA TATACTAAAA CTTATTGAAT TTTTTATTTA 1680
AAATGGGTTA AGGGTAAACC TTGCAGTATG TATATTAGAT CTCGATAAAG CAGTTTTTTT 1740
AAAAGGTGTA TTGAAACTGG GTCAAACACA CCAGAAGGGG AAGAACATCC CCAAGAGAGA 1800
GAAGAGCCTG GCAAACGCAT GGAGATGTGA ACCATCGCGA CAAGTAGGGG GACTGCCAGT 1860
CTTAGAGTGG CTGGAATGTA GGGTAGCTGT GGATGGCTCA AGTGTCCAAA AGGATTTAAG 1920
CAGCAAAATC ACAGAAACAA CTTCATTTTC ATGTAATGGC CCGAATCCCA GAGTCTCAAT 1980
GACATTCTGG GCACCTTCTG GTTTTTTGTT TTGTTTTGCT TTGTTTTTGA CTAAAAGCCC 2040
TTTCTCTGCC AAGTCTAAGA TGGGGAAGAA AGATGACGAG AAGGAAGAAC CCATATGCCC 2100
AAAGATTAGA ACAAAAAATA CATTTTCTAG AAATCATTTT GGTCATCTCT CTGCTTCTAG 2160
GCAGGTTTGT TAAACTAACC CAGACAGAGG AACCCATTTT GTCCTTAAAG GTCCCTAGAG 2220
AAGGAGACTC CAAGTGGGAC AGGCTTTAGG CTAAGAAAAA GCATTCTCTG CAGGCCCTTT 2280
GCAAATCCAG CCACACATGG AAAGCCCCTA AGAGAAGCAG AATGCCCTCC CTGCATTCTG 2340
ACCTGTTCAT GCCAGCCTAG TGACACGAAG CATTGATGTG AGGCCCTTGT TTCTTCAGTC 2400
ACCCAGCCCA GAATGCCCAG AGGAGGTAAA GATCACTTAC 2440