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

TagContent
EnhancerAtlas ID
HS020-09560 
Organism
Homo sapiens 
Tissue/cell
CD34+ 
Coordinate
chr12:6321900-6324240 
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
EWSR1-FLI1MA0149.1chr12:6324159-6324177TCTTCCTGCCTTCCCACC-6.28
Gata1MA0035.3chr12:6322201-6322212TCCTTATCTGT+6.14
Number of super-enhancer constituents: 44             
IDCoordinateTissue/cell
SE_00985chr12:6323657-6326136Adrenal_Gland
SE_01613chr12:6320234-6327226Aorta
SE_02955chr12:6320970-6322404Bladder
SE_02955chr12:6322433-6323544Bladder
SE_03308chr12:6322971-6323440Brain_Angular_Gyrus
SE_03308chr12:6323905-6326468Brain_Angular_Gyrus
SE_03988chr12:6322445-6326568Brain_Anterior_Caudate
SE_04905chr12:6320205-6328241Brain_Cingulate_Gyrus
SE_05857chr12:6318642-6328560Brain_Hippocampus_Middle
SE_06790chr12:6318775-6328722Brain_Hippocampus_Middle_150
SE_07876chr12:6320219-6323222Brain_Inferior_Temporal_Lobe
SE_07876chr12:6323483-6328413Brain_Inferior_Temporal_Lobe
SE_23086chr12:6320271-6323484Colon_Crypt_1
SE_23086chr12:6323578-6327203Colon_Crypt_1
SE_23760chr12:6321189-6322663Colon_Crypt_2
SE_23760chr12:6322715-6323215Colon_Crypt_2
SE_23760chr12:6323720-6326482Colon_Crypt_2
SE_24754chr12:6321035-6323561Colon_Crypt_3
SE_24754chr12:6323673-6326499Colon_Crypt_3
SE_25881chr12:6323668-6326767Duodenum_Smooth_Muscle
SE_26531chr12:6318963-6328738Esophagus
SE_27879chr12:6321701-6322570Fetal_Intestine
SE_31631chr12:6323508-6327264Gastric
SE_33937chr12:6322099-6328544HCC1954
SE_34881chr12:6323562-6327275HeLa
SE_35850chr12:6321445-6329804HMEC
SE_37830chr12:6323889-6326836HSMMtube
SE_37940chr12:6320586-6323707HUVEC
SE_37940chr12:6323743-6326586HUVEC
SE_41591chr12:6322625-6323332LNCaP
SE_41591chr12:6323706-6326500LNCaP
SE_42122chr12:6323541-6328356Lung
SE_44470chr12:6322576-6323518NHDF-Ad
SE_44470chr12:6323823-6327114NHDF-Ad
SE_48662chr12:6323814-6326216Right_Atrium
SE_50072chr12:6320199-6326579Sigmoid_Colon
SE_52457chr12:6320397-6322249Small_Intestine
SE_52457chr12:6323767-6326666Small_Intestine
SE_53862chr12:6323906-6325839Spleen
SE_54512chr12:6320070-6346293Stomach_Smooth_Muscle
SE_57526chr12:6323572-6325430VACO_503
SE_64246chr12:6320144-6328522NHEK
SE_68793chr12:6321228-6322414H9
SE_68793chr12:6322557-6326267H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr1263224366322600
Number: 2             
IDChromosomeStartEnd
GH12I006211chr1263202566322214
GH12I006213chr1263222806345639
Enhancer Sequence
GGGTAGGTAC CATAATCATC TCAGTGTCTA GAGCACTAAA TGGCCACAGA AGGCAGAAGT 60
TGGCCTCCCC AGGGACCCAG CTTGTCATGG AATGTTGGGT TTAAGTGTAT GTGTGGACCC 120
CTCTCCCCAG CCTGCCCTTA TGGTATAAAA GAGTGACATA TAATAGCAGG GGCCATTTAT 180
GACCCAGGGA CATTGCTGGG GTTGGGGGGA GTGGGCCAGG AGCGGGCAAG GAGTTGTCTT 240
GATAGAAACG CTGATTCCCG TGGGGAGACA GCAAATTAGT CACTCTCCTT AAGCCTTACT 300
TTCCTTATCT GTGTAATGAA GGTAATAACA CAACCAGCGT CTTACGATTG TTACTGGGAC 360
TAAGGGGATA TTTAATGTAA AGCTATTATA TGGGCCTGGC TCACAGGCAG AGCTTCTGTG 420
TTAGCTTCTG CTGCTGTTGC TGTAGTTGCT GCTACTGGTA CCTCTCCTTA ACATTTTTCA 480
CAGATTGAGG TTGTCTAAGT GTTCACATTC ATCCATATCT TCTCACTTCA GTTCATGAAA 540
CCACATCACA CAAGATCAGT CAATGCTGAA ATTTACCTCC AGTCTTTCTC CCTCTCGAAC 600
ACGAATTGGA GGACGTATCT TTCCACCTGT CTATAAAACA CTCATTTCTG AGACTTCCCC 660
AGTTTGGGGA AGACGGATAA AGAAGGGAAT CAGTTTTGCA CTTTGCTGGA AGCGCCTGTA 720
AGAATGCCCC ATTGGCAGAG ACTCGCTTTG TGGAGCTCAA CTTGGAAATT AATTTACAAT 780
GGAAATTGAA GGAAAATCTA CTTCATGTCC ACACCAAGAA GGGTGGCCTC AATGCCTCTC 840
CTTCAGTTCA CTCCTTGTGC CTTCCAAAAG GAAGTTGATT CTTCGTATGT AGAATTTTCT 900
GGACACCTAG AACACCTACA CCCAGAAACC AGGTCCCAGA GAGATGCAGA GCCACGGTCA 960
CCATTGCTTG TGTAGACACC AGGGGTAGGA AGTGGAAGGA AGGTAGCGCC TGAGGGTGCA 1020
GCTTCCCAGG GACCACCACC TCTCCCAGCC TCAATGGCGG GAGAGAACAA ACCCAAGGGA 1080
GAAGCTACGG GCCAGCATCT TCCCTCCCTC CCTCTTGGCC CCCACCAGGG CTAGGGTCAA 1140
CACCCCAAAT TGAAAGCATC TGTTGTCAAG CTGCAGCAGG CAGGGAAACC CTGTCACCAG 1200
GTTAAGGCTT AAGTCAGAGC ATTTTGCCAA ATTCAACACG TCCAAGCCTC CCACTTGTCC 1260
CCCAAGAAAA TTTCTCAGGG ATTCACATCT TTCCCAGTCA CCCCCTGGCC AGTGAGGAAG 1320
CACCGTGCAT CGAGAAGAGC ATAGCTTTGA GTCGTCTATG TGGAGCTGGT TCCATCTGAG 1380
CTCTGCCTCT TCCTGGCTGT GTCTTTTTGA GTCAGTTGCT TAAAATCTCT GAGCCTGATT 1440
CATCCATAAA ATGAGGGTGA TGAGAGGATT CAGTGAGAGA CTGTACATAA ACCACCTCCT 1500
GTAATGTGTC GGGGGCGTGG GTCCTTGTAC ATAGTAACTT CTACTGTTAA ATTGCTACTG 1560
TGGTGTTATT TTCCCTAAGC TAGACAACCT GCAACTTGAC CATTAGCCTC TTTTTTTTTT 1620
TTTTTTTTTT TTTTGAGATG GGGTCTCTGT CACCCAGGCT GGAGTGCAGT GGCGCAGTGT 1680
CAACTCACTG CAGCCTTGAC CTCCTGGATT TAAGCCATCC TCCTTCCTCA GCCCCCCAAG 1740
TAGCTGGAAC TACAGGCGTG TGCCACCATT CCCAGCTAAG TTTTTGTATT TTTTAGTAGA 1800
GACTGGGTTT TACCATATTG CCCAGGCTGG TCTCCAACTC CTGAGCTCAA GCATTCCGCC 1860
CCCCTCTCAG CCTCCCAAAG TGCTAGGTCA GGTCAGAGGC CTGACCATCA GCCTCTGAGT 1920
GTATTCTTTT AAAAAATTGT TTTTCTAGAG TTCGGGGAGG TTTGAGGAGA AGTCCAGTCT 1980
CATGCATAAC AGCGAGCTGG CCTAGGGAGC ACAGCCGGCT GCAGAATTCA GGGGGGAGGT 2040
TCTTACCAGG AGTGCCCTGC TGCAGGTTGT GGGAGCCTCT CACGGGCCCA CTGAGTCACC 2100
AGGGCCTGTT ACCAGAGGAG AGTTCACGCA GGCAGGGCCT GGGTGGTGGA TGTGCATTTG 2160
GGAGCCAAAC GCAGGTTCCA ACTTGAGCCC TTTACCATGA CTTCCTGGCT CAGTGGGTTC 2220
AGCACAGAGT TGTCCAGCCG TTCTCTCTCC TTTCTTACCT CTTCCTGCCT TCCCACCTCT 2280
CTGCATCCTC ACCCTTAATG GTCACAATGC CGCATTTCCA GGGTGACCCC AGGTTCCCTC 2340