EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS139-47094 
Organism
Homo sapiens 
Tissue/cell
Myotube 
Coordinate
chr6:41672360-41675570 
SNPs
Number: 2             
IDChromosomePositionGenome Version
rs6933790chr641672769hg19
rs35985639chr641673580hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CTCFMA0139.1chr6:41673790-41673809CCACCAGGAGAGGGCGCTC+6.15
RREB1MA0073.1chr6:41674227-41674247CCCCCAACCACCCTTACACC+6.16
Number of super-enhancer constituents: 33             
IDCoordinateTissue/cell
SE_01517chr6:41672610-41675135Adrenal_Gland
SE_03162chr6:41669606-41677521Brain_Angular_Gyrus
SE_03890chr6:41665119-41683317Brain_Anterior_Caudate
SE_04788chr6:41649933-41686942Brain_Cingulate_Gyrus
SE_05789chr6:41649369-41686280Brain_Hippocampus_Middle
SE_06686chr6:41649864-41686188Brain_Hippocampus_Middle_150
SE_07757chr6:41649397-41686150Brain_Inferior_Temporal_Lobe
SE_08794chr6:41672537-41673699Brain_Mid_Frontal_Lobe
SE_08794chr6:41674393-41675157Brain_Mid_Frontal_Lobe
SE_10407chr6:41671523-41677026CD19_Primary
SE_10977chr6:41658732-41703851CD20
SE_20329chr6:41672018-41676486CD56
SE_24100chr6:41671806-41674229Colon_Crypt_2
SE_24100chr6:41674949-41675560Colon_Crypt_2
SE_27512chr6:41672587-41676218Esophagus
SE_28789chr6:41672135-41674388Fetal_Intestine_Large
SE_28789chr6:41674541-41675608Fetal_Intestine_Large
SE_32569chr6:41671904-41676607GM12878
SE_40921chr6:41671436-41676757Left_Ventricle
SE_42849chr6:41672138-41676797Lung
SE_48161chr6:41672038-41677147Psoas_Muscle
SE_48786chr6:41672454-41676737Right_Atrium
SE_49598chr6:41672983-41675241Right_Ventricle
SE_50457chr6:41671880-41676685Sigmoid_Colon
SE_51489chr6:41672190-41676501Skeletal_Muscle
SE_53720chr6:41672566-41676702Spleen
SE_58883chr6:41671378-41704020Ly3
SE_59865chr6:41670633-41703769Ly4
SE_60547chr6:41671030-41704212DHL6
SE_61043chr6:41671264-41704230HBL1
SE_61929chr6:41668086-41703943Toledo
SE_62316chr6:41671424-41703890Tonsil
SE_65465chr6:41672391-41676432Pancreatic_islets
Number: 1             
IDChromosomeStartEnd
GH06I041704chr64167177841676629
Enhancer Sequence
TCTGCATTTT AACAAACTGC CCTGGGAGAT GTGTGGGCAC ATTAAAGACA CTTTACTTGT 60
TGCCTTCTGG GGACTTAGTT CCCTGGTTCC AAGCATGAAA ATTGGTGGCG GGTGGGAGAA 120
CACAGCAGGG AAGCACAGGC CCCTGGTGGA AGCACAGAGC TATTTTAAAG GACAGGCAGG 180
GCCCTTCTGA GCCCCACAGG GAAATTAAGC AGCCTGATTC TCAGGCTCAA GAGCCAAGGT 240
GGAGGCCAGA ATGCAAGGCT GCAGGTGGGC TCTGGCTCAC TGGGTGCTGG GGCTCTGGCC 300
CGTGCAGGAG GGGAAAACAA TCCAGGTCTA TGGGGAAACA GCTTCAAAGC CGAGATGGTT 360
ACCAGTGGAA AAGCAACCCA GACAGACCAT ATGAGACACA CCCATTCATG CAAACACCAC 420
CTCTCACACA TAAGCCACTG TCCACACATA CACACTCACC AGTACACACA CACTGCACCA 480
GGACTTGCCT GCCTGCCCAA AGAGCAGCTC CAGAAGAGAG CAGACAACCT TTGGGACAGT 540
GTGTGCCTGG GCCTGTGTGC TCCGCAGGAG GCCTGGGAGT GTGGAGGCTC CCACAGCAGG 600
TCTAGGAGCC CACTCTCTCC TCCACACGGC TCTGCCTCTG CCTCCCACCT GCCTAAACCC 660
CAGCTCCATC TGAACAATGA GAAACCTACG TCCTGCCCAC CTGAGGTTGG CAAGGACCCA 720
AATTTTAATT GGTCACCTGC CTGCTGACTC CCCTCTCCCC CAGTATACCA CCATCCTCCT 780
CACCAGGTTG CTGGGGGGTA ATCAGCAGAG TGGAGCTCTG ACTTCAGGGT TCCCTGAGAG 840
GCAGCCATAC CGCAAGGCCT GTGCCCACTC CCATGTACAC TCACACGGGA CAGCTGTAAA 900
GTCCACCCTC TTCCCAACGA CACAGCTTCT GAAGGGCCAG GGACCCTCAT CCACCCTGTC 960
CATGAAGAGG TGACAGCTCT CAACTCCACA CCCATTTTCA GCTCAGAAAC ACACATCCAC 1020
TGACCTCTTT CACCACCGCA GGCTGGACCT CTTCCACCAC CACAGGGCCC CCCAGGCTCA 1080
GATGGGCTCC AAAGAAACCC TAAATCATGG GGCCAGAATC CCAAGCAGGC CTAGGATGTC 1140
CAAAAAAGAA CCATCAACTA GGGAGGGTCA GTCTGGTCGC AGCAGGGTGT GTGATTTCAT 1200
GGGTTCTGGA AAGGCCCTCG GCCCCAAAAT ATCTTCCCTC TGGGTCCGGA AATCCCTCCC 1260
AACCCTCAGA TTCACTGCCG GGAGAGGCTC CCACCTGAAG CTCTCGTCAG CTCACACCCC 1320
TGGGAGAGGC AGCTGACAGC TGGCCTGAGA GCGGCCAAAG ATGGGCGGGG GAGAGTGGGT 1380
GCCAGGCCTG GTGACCGTCA TCTCGCCAGG GCCGCCCTGC CCACGAGTTC CCACCAGGAG 1440
AGGGCGCTCT TCCTCCCCAA CCCCAGAGCG CAGGTCCCCA GAATCCAGCA CCTCTGGCCA 1500
GGGAGAGGGG CCTAGCAAGG ACAGGGGCCT CAGCATGGCC TTCCACGTCC ATGCCAGGGG 1560
AAACCAAGGC CTGCCCCAAC TGTCCCCTTG AGGAAGCTGA AGTGCCAGAC AGCTGGAGGG 1620
GATGGGAGCC CTGAGAGCAG GGAGGTGGGG GGCAGAAGGG GGAATTAACC AGGTTCCAAA 1680
ATAGCAGAGT TGGTTCTGCC TCACTTCACC CTGTGCAGTG TCTGGCAGCT TCTGCTTTCG 1740
ATCTGAGTCA CGCCTGGTGG GGGCAGGACG GGGCAGCCAG TGCTGGCAGA GGCCACTAGA 1800
CAGCACAGGC AGTGGCCCAG GAACTCAGCG GGGGCTCTTC TCCCCTCACA ACACACACCT 1860
ACACCCACCC CCAACCACCC TTACACCCCC CCACCCCCAT CCTGCCCAAG AGTTGGGGTT 1920
CTGGGAAGAG CTAACAGGGG CCCACCCCAG GATTCCCAAA TGCTGTCAGC TGCCCTAGAC 1980
CCAGAATTCA GCTTTGCTCC TGCCCTGTCC ATGTGCGCTC CGGCTGGCAT TCCCACCCCA 2040
TCTCTGTCAG GGAGCCAGAG GAGGAGACCT GACCTGGAAG CCACCATCTC CCCCCATAGA 2100
GGAGAAATGG CCTCCTATGG CAACATTCCA ACAGCCCACC AAGTCACCCA CCCACCGGAT 2160
GGAGTGAGTG AGCTGTCCCC CAACCTGCCC CCATCTCCCC CCGCCCACAC CCAGGTATGA 2220
AAGGAACAGG AAGCAAAATT CACACACACA CACTTCCAGC CCTTTTCCTG TCCTTAAACA 2280
CCATAAGAAG CACTCTGCCT TTACCAGGAC AGAGCGAGGA GTGGGGTGTG TTGAACTCTG 2340
CATGTGATGG GGTCGGGGGA GGAGCATCGG GAAGTCTGCT CTTTCATCAT CATTCTCTTC 2400
CACTCATCTG GGCTCCATGC CCTCCTGCCT GCCCAGCCCC AAGGCTCAGA GCTGCTCTGC 2460
TTTCCCCCAT AGAGTTGAGA CTCAGGCAGC AGCTGCCTTA CACCTTCTCC CTGGACCCAA 2520
GATGCTTGAG CTCAAACCTG AGACATAAAC CCCATCTTCC AATGCCTGAA CCAATCCTCT 2580
CTGTTCTCCT CCCAACAACA CACCTGCCTG GAGTGAGTGC AGCCACCTTC CTATCCAAGT 2640
GGCGGAGTGG GGAGATGATA GACTCGGGCT GCCATGGCTG GGCCTGCCCA CAGGGTAGGG 2700
AATGGCACAG GCAGACACAC TCCTACCCCT GCCACCCCAG CACACGCACC CAGAGCAGAC 2760
CTGGTTTGGA AATGAAACAT CAAGGGGAAA GGCTGGGGCT GGTGGCTGGA GGAAGAAGTC 2820
AGAGGGGCTG TGACTTGGCG TGCCTGCCTG TGGCCCAGGA CCACGTCTCC AGGGGAAGCA 2880
CACCGCCAGG CCCAGCCCCT GCCCCATCCC CATCTCCTGC CCTTCCCCTA GCCCCCACCC 2940
CAGAAGGCCT TACCTACACG CCACTTCCCT CTTTTAATTC TTCCCATTCC CTCAGCCCTA 3000
TAGGGTGCGA GACCTGTAGC CTGAAGCTGG GAGGGCTGGG GATGGGAACA GGTGGAGCCC 3060
AGGGGAAGAA GGCTCCTCTC CAAGAAGCAG ACATGACAGA GCCTGTGCCA GGGCAAACAG 3120
GTATGCCACC GCACGAAATT ACTCCCCCAC CAAAATGTCC CTGAATTGTA TCCTGTTCCT 3180
GACAGAGACA CAGAGGGAGG CTACTAGGAG 3210