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

TagContent
EnhancerAtlas ID
HS101-00908 
Organism
Homo sapiens 
Tissue/cell
HT29 
Coordinate
chr1:27885400-27887660 
Target genes
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
ZNF263MA0528.1chr1:27887446-27887467TCCCTCTTCCCTCCCTCTCCC-6.06
ZNF263MA0528.1chr1:27886273-27886294TCCTCACCACCCCCCTGCTTC-6.41
ZNF263MA0528.1chr1:27887452-27887473TTCCCTCCCTCTCCCTCCCTT-6.41
ZNF263MA0528.1chr1:27887457-27887478TCCCTCTCCCTCCCTTCCTCT-6.68
Number of super-enhancer constituents: 47             
IDCoordinateTissue/cell
SE_00861chr1:27886075-27904718Adrenal_Gland
SE_01588chr1:27880381-27885646Aorta
SE_01588chr1:27886149-27904879Aorta
SE_03261chr1:27886890-27888097Brain_Angular_Gyrus
SE_03939chr1:27883710-27885742Brain_Anterior_Caudate
SE_03939chr1:27886198-27895237Brain_Anterior_Caudate
SE_05478chr1:27885928-27895152Brain_Cingulate_Gyrus
SE_05814chr1:27880294-27902223Brain_Hippocampus_Middle
SE_06945chr1:27886514-27895216Brain_Hippocampus_Middle_150
SE_07770chr1:27881026-27885690Brain_Inferior_Temporal_Lobe
SE_07770chr1:27885748-27895172Brain_Inferior_Temporal_Lobe
SE_08953chr1:27887161-27887433Brain_Mid_Frontal_Lobe
SE_14757chr1:27885672-27892439CD4_Memory_Primary_7pool
SE_23479chr1:27883335-27885708Colon_Crypt_1
SE_23479chr1:27886596-27887635Colon_Crypt_1
SE_24168chr1:27883426-27885642Colon_Crypt_2
SE_24711chr1:27886607-27887112Colon_Crypt_3
SE_24711chr1:27887184-27888248Colon_Crypt_3
SE_26518chr1:27880547-27885700Esophagus
SE_26518chr1:27885702-27904919Esophagus
SE_27625chr1:27882781-27885755Fetal_Intestine
SE_27625chr1:27886768-27889100Fetal_Intestine
SE_28547chr1:27882782-27885683Fetal_Intestine_Large
SE_28547chr1:27886814-27889082Fetal_Intestine_Large
SE_29557chr1:27886726-27904956Fetal_Muscle
SE_31394chr1:27880792-27885806Gastric
SE_31394chr1:27886081-27904513Gastric
SE_33503chr1:27886818-27904912H2171
SE_34367chr1:27883153-27885684HCT-116
SE_34755chr1:27882745-27885799HeLa
SE_39896chr1:27886141-27887643K562
SE_40593chr1:27885841-27904966Left_Ventricle
SE_42106chr1:27880393-27885776Lung
SE_42106chr1:27886079-27904957Lung
SE_46630chr1:27886679-27892191Ovary
SE_48058chr1:27885887-27904727Psoas_Muscle
SE_48567chr1:27886102-27904727Right_Atrium
SE_49444chr1:27886820-27892209Right_Ventricle
SE_50130chr1:27880522-27885676Sigmoid_Colon
SE_50130chr1:27886169-27892585Sigmoid_Colon
SE_51091chr1:27886184-27904991Skeletal_Muscle
SE_53892chr1:27886040-27904947Spleen
SE_54527chr1:27885939-27904929Stomach_Smooth_Muscle
SE_65253chr1:27884396-27885784Pancreatic_islets
SE_65253chr1:27886204-27900313Pancreatic_islets
SE_68682chr1:27883179-27885755H9
SE_68682chr1:27886365-27891995H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr12788675727887000
Number: 2             
IDChromosomeStartEnd
GH01I027554chr12788064127885661
GH01I027559chr12788613127905256
Enhancer Sequence
AAGCAAACAC AGCACCACAG AGATAAGCAT GGACACAGGG TAAGCCAGCC AGACAGCAGG 60
GTGCAGGCGG ACACTGAGCC AGGAAGCTCT CCTACATGGA GTCCCATCCA CCTCCAACCT 120
CATCGCATTA TCCCACCTGG GAACTGTGAG ACTCTTTTTA AAAAAAAAAA TAAGAGAGAC 180
AGGGCCTCAT CTCGTTTTGT GGCCCAGGTT GGAGTGCAGT GGCATGATCA TAGCTCACTG 240
CCTCCTTGAA TTCCTGGGCT CAAGTGATCC TCCCACCTCA GCCTCCCGAG TAGCTGGGGC 300
TACAGGTATG CACCACCATG CCTGGCTATT TTTTTTTTAA ATTTTTTGTA GGGACAGGGT 360
CTCACCATCT TGCCCAGGCT GGTCTCGAAC TCCTGGGCTC AAGCAATCCT CCAGCCTCAG 420
CCTCCCAAAG TGCTGGGATT GCAGGTATGA GCCACTGCAC CAGCCAAACC TGTTTCTTGA 480
AACCCCAGGC TCCTACTGAG AAGCAATGTT TTTGCACATC TATGTACACA CATGCATATA 540
CATGCACATA TACTATAGTG GAAGGAACCT GGCCTTTGGG AGTCTGACAG TCCTTGGCTC 600
AACCTTCATA ACTGTGTGAC TCTGGGCAAG TCAGTTAACT TTTCTGGCTC TCAGTTTTCT 660
CATGTATAAA ATAGGAAAAG TGAGATCTTA TGAATGGGGA GGAACATCTG GGGAAACTAT 720
AATGCAAACA GGTTACTGAC AATGCAGATG TGAGAGGTGC TGTTCAGAGT GATGGTGGAT 780
GCGAATTTCC ACAAGGGTGT ATATGCAGCT GGCGTTTACC CATTTCCATC AGTAACTAGT 840
TATGTCTCTT GTTTTCTTTA ATAACCATGG CCCTCCTCAC CACCCCCCTG CTTCCTGCCC 900
ATTTGTCTGC CTCCTCGAGG TCTGTACTGG AGCCCAGAGG GGGTCTGGGA ACCAGGCCTC 960
ACGGATTGCT TATAGGTTCT GGTTGCCTGG GAGTTTGTAT GCGTGTGATC GAGATTCTGC 1020
CTGTGCAAAT GCATATCTGT CAAGGCTCAG CTGTCTGGGT AAATATACCT GTATGTGGGT 1080
TCCTGGGTCT ATTTAGCCTG TTCGTGTGCT TCTCTGTATT TCTGTACGTC TGTGTGGGTA 1140
CATGTGGGCT TAAGCGTGTC CATGTGTGGG ATCACGCGTT TGCTCAGTTG TGGCTGCTGT 1200
GGTCAGCTGT GTGTGTGTAT GTGTGATGCC AGCTTAAGTG TGTGCCTGGA TTTGGTGTCT 1260
TCAGTCATAC ATGTGGGTAT GTGCACTTTT CACGTTTATT TCTATTCGTT TTGTGTGTGT 1320
GTGTGTGTGT GTGTGAGTCT AGCTAAGCCT GTTTGTGTGT GAGGACACAG GGGTGCATGT 1380
GTGCCTGTGT GTAGCCAGGT GAGCCCAGCT GTGGCTGGGT GTGAGCATGC CTGGGTGTGC 1440
ACACGCTTTG CCTGGCTCTC TGCATCTCGC TGTGTCAGGA GCCAAACCGG CTCCTGCCTG 1500
TCTCAGAGCT CTCTGGATGT GTGTTTGGCA GGGGGTGGGG GCGTGAGGCT GATCCTCTGC 1560
TGTCCCTGCA GGTTTCCAAT CTCGAGGCCT GTGACTGCAG GCACTGGTGT CACTGTGGAT 1620
CAGTGTTGCC TCCCTCCCAC CTCTGCCTTT CTCTGGGTTT TCAGGGTCAT GGTGTGGCAG 1680
TGTGACTGGC CACAGTGTCC CTGTGGGTCT CTTTCACCAT GGGTCAGTAT GTGCTCGTGT 1740
GTGTGTCCAT GCATGTGTGG ATTTGTGTGA CCTTATTGTG TGTCTGTGTA CCACAGCGTG 1800
TCTCTGTGTA TGTCAGTGGG TCCTTGTGCT ATGTCACTGT ATGATTGTGC CAGTATGGCC 1860
GTGTGTCAGC GTCAACATGT GTGAGCAGGT CTGTGTGCCA TGGTGTGTCA GCACAACGGT 1920
GCCCCAGGGT TTGTGTGGTA CCTTTGTGAA GGGCTCAGTG TGTGAGTGCG TGTGTGCATG 1980
CATGTGAGAT ACCCTTTGTG AGACGGTGTG TGTGTGTCTG TGTCACTGTG TTTGTGTGTG 2040
CCTGCTTCCC TCTTCCCTCC CTCTCCCTCC CTTCCTCTCT CTCTCTCTCT GTAGGAGCCA 2100
GACAACTCCC CAAGCCTGGA TTAGGGACAA TTTATCCACA GGCAGAGAAG GAGAATTCCA 2160
ACCTGCCAGA GCCTCCCTCC TCTGATCTGT CCCCCCTTTC CCTGTGGTTG GGTGGGCACA 2220
GAAACACAGC CCGGCAGCTC CCAAGCCCTT GGGGAGCCCC 2260