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

TagContent
EnhancerAtlas ID
HS098-12422 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr12:12889510-12891780 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11055034chr1212890626hg19
TF binding sites/motifs
Number: 3             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
FOXC1MA0032.2chr12:12891449-12891460ATATTTACATA-6.62
FOXF2MA0030.1chr12:12889639-12889653TTAACATAAACAAT+6.03
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
AATAAATTTT ATTGTTTCCT CACTTTATCT AATATTAATT GAAATCCTTA GTCTTATGTT 60
GGGGTTATCC CAATAGGACG TGGGAAAGAA AGTTCAAGCT TTCGCCTTGA TAGTTCTCCA 120
TGATGCTGCT TAACATAAAC AATCGAGTTT TCAAAAACCA AAACTCTTGA TTTCATTAAG 180
TAAGGAGGGT GTAATGTGTA GTGCTTGGGC CGTTAGAGGG GATGTGGTCA CAAGTGGTAT 240
ATCTGAGGCT TTTGAAGGAG TGCATTCAAG GAAGAGCCCT GCTTGGTGTC AGCTACTGAA 300
CCAGAGATCC GAAGAAGTGG ACCTCGCCAG CCTCCTGCTC CACCCCGCTA CCAGTCTTAG 360
CTGGAGCTCC CTTTTCTTTG TCATACTCAG CCAGTTGCTC ATTGCTGTTT TAGAGTCTGG 420
CCCATGTTTT GCTCTTTGGC TGTGCGATTG GCGTGAATCT TCTAAGCAAA TGAATAGCTT 480
AGAGGTGAAT ACTGAATCTT TTGCTTCAAG TAGCTCAGCA TTTTTGTCTT TCATTTTTAC 540
TAAGTGACTA GATTCAGTAT TCGAAGATGT TTTGGCCAAA TGATTCATTA TTTATTTGGC 600
TTTAGAAAGA GACTTCAAAA GGATAATAGA AATAAACAAC CCAGAGGTTT TTTTTTTAAA 660
TTGAAGATTA ATAAAAGAGA GACCTCTGCT GGCTACAGTG GGGTAACAAC CTAGAGTTGG 720
CCACTGACTC CACAGGAAGC TATAATGGCT GTGACCCACC CCATACGCTT TTACAGTTGT 780
CAGCAAATTG ATCACTATTT GTTCACTTCT TCAGCAATCA ACTCAAGTTC TTTTGGAGTT 840
CATTGAAGTG AGGTATAATT CCCAGTCCAA TCACCACTGT TTCTGTTTCA ATCTTTAGGA 900
AAAGTATTAG TCTTTTATAT TTCTCGAACA TAATAGCTTT ACATATGAGC CCCTGCCAAA 960
CTGAGACCTG AAATAATTCC TGCATCTTAC CTTCTCTGTT TCCTTTCCCC TTTTTTGCCT 1020
CCACCTCTCC TCCTCCCCTT CTCCAGTAAA ACAAAATAAA ACAAATCTAC ACTCAAGAGA 1080
GAGTACTGAT AGAAAGTGAG AAGGAGGGAG CTGGGCGCTT ATCTTTGGCA TATCCTCAGC 1140
TGAGGATCCA AGCTGGGGGG CCCAGGGTTG GTGTTAACTA CCTGAGTAGA GCTGTAGTTC 1200
CTACTGATGT CTTCCGTGGG ATTTGTTCAA CCGTGGGAAT GTGGCTGCAC GATAGTGGAG 1260
CAAGATTCAG TGAATGCTTC AGAATATGGA GGGTCGTTAT CTAGGGGGAG GAAGGGGACT 1320
GAATGTTCTC TTGAGACCTT TTGTTGGCAA CAACAATAAT GAGTGCCTAC TATGTGCCAG 1380
GCCCTGGACT AAGTACCTTA AATACCTTAA TTCTGTTTCC TGCTTTTCTT CTCTCTTCAC 1440
AGTCTTAAGA ATGTCTTTCT ATGAGAAAAA CATTGAATAT ATGTAAAGAA CTTACAACAA 1500
GGCCTGCATA AAGTAGTAGC TATGCATGTG TTCACTATTT TATTATTATG TTTTTACTCT 1560
GGAATATGCT GCCACTCCTA CACATGAGGA GAGGCTCTCC CCATACTCAC CAGAGCAAGC 1620
AAGTCCTTTT TTTTTTTTTT TTTTTTAAGA CACATGGAGT CTTGCTCTAT TGCCCAGGCT 1680
GCAGTGCAGT GGCATGATCA TGGCTCACTG CAGCCTCGAC CTCTTGGGCT CAGGCAGTCC 1740
TCCTGCCTCA GCCTCCTGAG TAGCTGGGAC TGCAGGTGTA TGCCACCACA CCTGGCTAAT 1800
TTTAAATTTT TTAGAGATGG GGTCTCACTA TGTTGCCCTG GCTGGTCTTG AACTCCTTTG 1860
CTCAAGCAGT CCTCCCAACT TAGCCTCCCA AATCATTGGG ATGAGAAGCA TGAACCACTG 1920
TGCCTGGTTA ATTACATAGA TATTTACATA TCTACTATCT TAAAACGGTG TCCTTTTAAG 1980
AATTTCAAAT GATGCTTTAT AGTTTCTAAT ATGGTGCACT GGGTATACTG TTGATATTTA 2040
AAGTTTTGTG AATGATAAAT TTCCCTACTT CAGTAGTGCC ATAGAATTAA TTGATTCTTG 2100
TATCTGAAAT TTAATGAGTG CTTATGAAGT ATGCTGGACT GTGCTAGGTT CTGACAGCAT 2160
TTGAAAAGAA GTTTGACATC TGCCTGTCTG TCCCCTTTTG GCTGCCTATG AGGTGTGTAA 2220
GATGGCTGCA ATTTGAGGAG GCATCCTTTG TTCCTGAGGA TAGAAGGTGC 2270