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

TagContent
EnhancerAtlas ID
HS105-17681 
Organism
Homo sapiens 
Tissue/cell
IMR90 
Coordinate
chr12:12889650-12892370 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11055034chr1212890626hg19
TF binding sites/motifs
Number: 2             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr12:12891449-12891460ATATTTACATA-6.62
ZNF263MA0528.1chr12:12890533-12890554CCTCTCCTCCTCCCCTTCTCC-6.17
Number of super-enhancer constituents: 45             
IDCoordinateTissue/cell
SE_02384chr12:12889367-12891080Astrocytes
SE_03015chr12:12889561-12890025Bladder
SE_04457chr12:12889399-12890487Brain_Anterior_Caudate
SE_05723chr12:12889250-12890996Brain_Cingulate_Gyrus
SE_06515chr12:12889295-12890622Brain_Hippocampus_Middle
SE_07055chr12:12889264-12890612Brain_Hippocampus_Middle_150
SE_09887chr12:12889463-12890550CD14
SE_10399chr12:12889466-12890156CD19_Primary
SE_11298chr12:12889288-12891024CD20
SE_11994chr12:12889317-12890964CD3
SE_13418chr12:12889451-12890667CD34_Primary_RO01536
SE_14411chr12:12889291-12890783CD4_Memory_Primary_7pool
SE_15395chr12:12889422-12890889CD4_Memory_Primary_8pool
SE_16327chr12:12889289-12890803CD4_Naive_Primary_8pool
SE_16955chr12:12889358-12890444CD4p_CD225int_CD127p_Tmem
SE_17376chr12:12889323-12890851CD4p_CD25-_CD45RAp_Naive
SE_19332chr12:12889413-12891128CD4p_CD25-_Il17p_PMAstim_Th17
SE_20110chr12:12889323-12891107CD56
SE_20780chr12:12889241-12890995CD8_Memory_7pool
SE_21484chr12:12889406-12890424CD8_Naive_7pool
SE_21956chr12:12889267-12891152CD8_Naive_8pool
SE_24059chr12:12889693-12890061Colon_Crypt_2
SE_25539chr12:12889286-12890978DND41
SE_25894chr12:12889266-12890640Duodenum_Smooth_Muscle
SE_26782chr12:12889510-12890129Esophagus
SE_27782chr12:12889424-12890846Fetal_Intestine
SE_31002chr12:12889358-12890247Fetal_Thymus
SE_31618chr12:12889585-12890095Gastric
SE_32681chr12:12889248-12890518GM12878
SE_34820chr12:12889520-12891049HeLa
SE_42460chr12:12889585-12890140Lung
SE_44374chr12:12889461-12890977NHDF-Ad
SE_44929chr12:12889526-12890707NHLF
SE_45697chr12:12889295-12892730Osteoblasts
SE_47372chr12:12889267-12891175Panc1
SE_50256chr12:12889478-12890056Sigmoid_Colon
SE_52464chr12:12889382-12890237Small_Intestine
SE_53337chr12:12889493-12890332Spleen
SE_55147chr12:12889567-12890034Thymus
SE_56035chr12:12889371-12890742u87
SE_61268chr12:12866751-12890857HBL1
SE_61621chr12:12866181-12890888Toledo
SE_62220chr12:12864939-12895381Tonsil
SE_66441chr12:12889534-12890218Jurkat
SE_67164chr12:12889427-12890439MM1S
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr121288973212889911
Number: 1             
IDChromosomeStartEnd
GH12I012733chr121288605512890944
Enhancer Sequence
AATCGAGTTT TCAAAAACCA AAACTCTTGA TTTCATTAAG TAAGGAGGGT GTAATGTGTA 60
GTGCTTGGGC CGTTAGAGGG GATGTGGTCA CAAGTGGTAT ATCTGAGGCT TTTGAAGGAG 120
TGCATTCAAG GAAGAGCCCT GCTTGGTGTC AGCTACTGAA CCAGAGATCC GAAGAAGTGG 180
ACCTCGCCAG CCTCCTGCTC CACCCCGCTA CCAGTCTTAG CTGGAGCTCC CTTTTCTTTG 240
TCATACTCAG CCAGTTGCTC ATTGCTGTTT TAGAGTCTGG CCCATGTTTT GCTCTTTGGC 300
TGTGCGATTG GCGTGAATCT TCTAAGCAAA TGAATAGCTT AGAGGTGAAT ACTGAATCTT 360
TTGCTTCAAG TAGCTCAGCA TTTTTGTCTT TCATTTTTAC TAAGTGACTA GATTCAGTAT 420
TCGAAGATGT TTTGGCCAAA TGATTCATTA TTTATTTGGC TTTAGAAAGA GACTTCAAAA 480
GGATAATAGA AATAAACAAC CCAGAGGTTT TTTTTTTAAA TTGAAGATTA ATAAAAGAGA 540
GACCTCTGCT GGCTACAGTG GGGTAACAAC CTAGAGTTGG CCACTGACTC CACAGGAAGC 600
TATAATGGCT GTGACCCACC CCATACGCTT TTACAGTTGT CAGCAAATTG ATCACTATTT 660
GTTCACTTCT TCAGCAATCA ACTCAAGTTC TTTTGGAGTT CATTGAAGTG AGGTATAATT 720
CCCAGTCCAA TCACCACTGT TTCTGTTTCA ATCTTTAGGA AAAGTATTAG TCTTTTATAT 780
TTCTCGAACA TAATAGCTTT ACATATGAGC CCCTGCCAAA CTGAGACCTG AAATAATTCC 840
TGCATCTTAC CTTCTCTGTT TCCTTTCCCC TTTTTTGCCT CCACCTCTCC TCCTCCCCTT 900
CTCCAGTAAA ACAAAATAAA ACAAATCTAC ACTCAAGAGA GAGTACTGAT AGAAAGTGAG 960
AAGGAGGGAG CTGGGCGCTT ATCTTTGGCA TATCCTCAGC TGAGGATCCA AGCTGGGGGG 1020
CCCAGGGTTG GTGTTAACTA CCTGAGTAGA GCTGTAGTTC CTACTGATGT CTTCCGTGGG 1080
ATTTGTTCAA CCGTGGGAAT GTGGCTGCAC GATAGTGGAG CAAGATTCAG TGAATGCTTC 1140
AGAATATGGA GGGTCGTTAT CTAGGGGGAG GAAGGGGACT GAATGTTCTC TTGAGACCTT 1200
TTGTTGGCAA CAACAATAAT GAGTGCCTAC TATGTGCCAG GCCCTGGACT AAGTACCTTA 1260
AATACCTTAA TTCTGTTTCC TGCTTTTCTT CTCTCTTCAC AGTCTTAAGA ATGTCTTTCT 1320
ATGAGAAAAA CATTGAATAT ATGTAAAGAA CTTACAACAA GGCCTGCATA AAGTAGTAGC 1380
TATGCATGTG TTCACTATTT TATTATTATG TTTTTACTCT GGAATATGCT GCCACTCCTA 1440
CACATGAGGA GAGGCTCTCC CCATACTCAC CAGAGCAAGC AAGTCCTTTT TTTTTTTTTT 1500
TTTTTTAAGA CACATGGAGT CTTGCTCTAT TGCCCAGGCT GCAGTGCAGT GGCATGATCA 1560
TGGCTCACTG CAGCCTCGAC CTCTTGGGCT CAGGCAGTCC TCCTGCCTCA GCCTCCTGAG 1620
TAGCTGGGAC TGCAGGTGTA TGCCACCACA CCTGGCTAAT TTTAAATTTT TTAGAGATGG 1680
GGTCTCACTA TGTTGCCCTG GCTGGTCTTG AACTCCTTTG CTCAAGCAGT CCTCCCAACT 1740
TAGCCTCCCA AATCATTGGG ATGAGAAGCA TGAACCACTG TGCCTGGTTA ATTACATAGA 1800
TATTTACATA TCTACTATCT TAAAACGGTG TCCTTTTAAG AATTTCAAAT GATGCTTTAT 1860
AGTTTCTAAT ATGGTGCACT GGGTATACTG TTGATATTTA AAGTTTTGTG AATGATAAAT 1920
TTCCCTACTT CAGTAGTGCC ATAGAATTAA TTGATTCTTG TATCTGAAAT TTAATGAGTG 1980
CTTATGAAGT ATGCTGGACT GTGCTAGGTT CTGACAGCAT TTGAAAAGAA GTTTGACATC 2040
TGCCTGTCTG TCCCCTTTTG GCTGCCTATG AGGTGTGTAA GATGGCTGCA ATTTGAGGAG 2100
GCATCCTTTG TTCCTGAGGA TAGAAGGTGC ATTGTGGAGT AGAAAGATAC AGGAACTATA 2160
GGCGATGCCA CACCAACTCT GTGCCACTTA TCTCCAGAAT TCCTGTACAG AAAAGAAAAG 2220
TACACTTTTA TCTTGTTTAA GCCACTATGA TTTCTGGGCT CTGTTACTAG CTGCCAAATG 2280
CAAATCTTAA CAGATACAGA AGTCCTTGAG GATTTTTGAG CAAGGAACTG ACTGTAAAAC 2340
TGGTGGCTCT GCAAGGGACA GATTTGGGGA GGGGGGTGTT CTGGAGAATC CTAAGAGATA 2400
AAGTTGGCTT GGTAGGTGGG GACAGATAGT AGGGGAGACT GAATGCGGAG AATACACATC 2460
TTGCACAGGT CACTGAATTT TGTTTCTTTT TCCCAGGACA CCTCTGCTAA ACTCCTATTT 2520
TTACCGTGGT TATTTAAATA TGTGGTTATT GAGGAATTTG TATTCTGCTA TCGTCAAGTG 2580
GCCTGAAAGC CAGGGAGATC GAGAAGATGA GTGTTCTTTG TGCTTTAAAA AGAAGCAGGC 2640
AAAAGCTGGA ACGGGAAAGA GTATCAGTGT TACAGTGAAG TGAAGTTACT ATGTTTTCTG 2700
AACTCCTGCA AGCATTTTCA 2720