EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS068-04938 
Organism
Homo sapiens 
Tissue/cell
GM18526 
Coordinate
chr6:111909920-111912460 
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
TGTATGCAAT GCTTGCCATA GCATTGCTTA TTGGATCAGA AAACTGGAAA CTATTTTAAA 60
TGTCCAACAA TAAAGAATAG GTTCATAACA ATTTGGTAGA TGCGTCTGAT GAAATACAAT 120
GAAGCAGTTT TAAATGATTC TGGAATAAGT ACTCAATGTC ACTGAAAACT ATTTTAATTT 180
TAGATTAAAA ATATATGCAA AGAAAAAAAC ACTGAAAATT GATATGTCAA AACCCTAATA 240
AGGAATTCTA TTTGGGTGGC AGAAATATGA AAACTTTTTC TTTTCTTTTT TGAACTTCTG 300
GGCATATTTT AATTTTGGGA GTGACCAAAT ATTATAATGA TCAGAAAAAT TATCTTTTTT 360
TTTTTTTTTT TTGAGATGGA GTCTCACTGT GTCATCGCCC AGGTGCAGTC TCGGCTCACT 420
GTAACCTCTG CCTCCCAGGT TCAGGCAATT CTTGTGCCTC AGTCTCCCGA GTAGCTGGGA 480
TTACAGGCGC CCGCCACAAC AACTGGCTAA TTCTTTTTGT ATTTTTAGCA GAGACAGTGT 540
TTCACCATGT TGGCCAGGCT AGTCTCAAAC TTCTGATCTC AAGTGATCCA CCCACCTTGG 600
CCTCCCAAAG TGCTGGGATT ACAAAGTGGG GTGAGCCACC GTGCCTGGTG AAAACTTACC 660
TTTAAATACA GATAACAGAA TGTTAAAAAG TAGTTTATGG TATTATTCTC ACAAATTACT 720
CCTTTTAAAC CTGGCAATCA CTGAGAAATA CAGCCTTGAC CTTGCCAACA TTCAGTTCTC 780
AGTGATTCAT ACTTAAGGGA ATCCACCACC ACACCCACCC TATGACTGGG CGCTTAGAGC 840
AGGGGTGGCA TCCATGCACT CCCACTCTGT TGACTTCCCA GCATTTATAC ACCACGTCCC 900
AGTTTTAGGC ATCAGAGGCT CTTTCTCCCG CTCCAGCCCA AGGCCCCATT CTCCTTACAC 960
CCTCCTGCTT CCCCAGCCCC TGCCCTCATT CCTGATCTCA CACTCATTCT TACCTATTTC 1020
TTCCAAGCAT CTTCTAAGTT ACATTTCTCT ATCTCCTCTT TGTTTTTTTC TTTTTTGAGT 1080
TATGAATTAC TGTGTTGCTC TCTTCACTTT AGGAAGCTTT ATACTTAGTA TACATGTACT 1140
AATATGTAAA TTATGGTTGA TTACAGCATT TGTAATTATT TCTATAATTT ATTTTAAAGC 1200
TGCGCATCAG GCCTTTGGTC AGGCACTTCT TACACTCTGA ACTACTTTCT GTCCAGTGTT 1260
TATTTGCTAA GAAAAATATC AGGCCTCACA GCCCTGTGTT TCATCTGTAA AGCCCTTTTG 1320
TTATTTTCCA GTGGCCTCAG CGGAGATTTA ACATCAAGAA TGGTAGTAGG AAAAAAAAAA 1380
TGGTGATAGA ACCTTTTATC TCAACCTAAG ACTTATCACT TTCAGAGATG CTTCCTGCAC 1440
TGATACATAT TATTATTTCG GAAGTAGTTT ATTGAGAGTC TAGTATGTGC CAGACACTGT 1500
GCTTAAATCC TGGGGAATTA TGAATTGAAA GTACACGTTT GCATTTGCAG ATGCATAAAA 1560
ACTTGCAGTC TAGAAGGAGA GGAGACACGT ACATAATTAG ATGCCATGCT GGTGTTAGGT 1620
GTCCCAACAG GGCCAGAGCA GGAGGGAGAC AGAGGCCCTG AAGGAGAACG TGATCTGGGG 1680
AGGTTTCCAG AGGGACACTT GAGCTAAGTC TCAAAAAATG TGTATGATGG TGGTTGCATA 1740
ACTCTGTAAA TATACTAAAA CTTATTGAAT TTTTTATTTA AAATGGGTTA AGGGTAAACC 1800
TTGCAGTATG TATATTAGAT CTCGATAAAG CAGTTTTTTT AAAAGGTGTA TTGAAACTGG 1860
GTCAAACACA CCAGAAGGGG AAGAACATCC CCAAGAGAGA GAAGAGCCTG GCAAACGCAT 1920
GGAGATGTGA ACCATCGCGA CAAGTAGGGG GACTGCCAGT CTTAGAGTGG CTGGAATGTA 1980
GGGTAGCTGT GGATGGCTCA AGTGTCCAAA AGGATTTAAG CAGCAAAATC ACAGAAACAA 2040
CTTCATTTTC ATGTAATGGC CCGAATCCCA GAGTCTCAAT GACATTCTGG GCACCTTCTG 2100
GTTTTTTGTT TTGTTTTGCT TTGTTTTTGA CTAAAAGCCC TTTCTCTGCC AAGTCTAAGA 2160
TGGGGAAGAA AGATGACGAG AAGGAAGAAC CCATATGCCC AAAGATTAGA ACAAAAAATA 2220
CATTTTCTAG AAATCATTTT GGTCATCTCT CTGCTTCTAG GCAGGTTTGT TAAACTAACC 2280
CAGACAGAGG AACCCATTTT GTCCTTAAAG GTCCCTAGAG AAGGAGACTC CAAGTGGGAC 2340
AGGCTTTAGG CTAAGAAAAA GCATTCTCTG CAGGCCCTTT GCAAATCCAG CCACACATGG 2400
AAAGCCCCTA AGAGAAGCAG AATGCCCTCC CTGCATTCTG ACCTGTTCAT GCCAGCCTAG 2460
TGACACGAAG CATTGATGTG AGGCCCTTGT TTCTTCAGTC ACCCAGCCCA GAATGCCCAG 2520
AGGAGGTAAA GATCACTTAC 2540