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

TagContent
EnhancerAtlas ID
HS076-12889 
Organism
Homo sapiens 
Tissue/cell
H1 
Coordinate
chr12:12889830-12891880 
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: 43             
IDCoordinateTissue/cell
SE_02384chr12:12889367-12891080Astrocytes
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_56035chr12:12889371-12890742u87
SE_61268chr12:12866751-12890857HBL1
SE_61621chr12:12866181-12890888Toledo
SE_62220chr12:12864939-12895381Tonsil
SE_66441chr12:12889534-12890218Jurkat
SE_67164chr12:12889427-12890439MM1S
Number: 1             
IDChromosomeStartEnd
GH12I012733chr121288605512890944
Enhancer Sequence
ACCTCGCCAG CCTCCTGCTC CACCCCGCTA CCAGTCTTAG CTGGAGCTCC CTTTTCTTTG 60
TCATACTCAG CCAGTTGCTC ATTGCTGTTT TAGAGTCTGG CCCATGTTTT GCTCTTTGGC 120
TGTGCGATTG GCGTGAATCT TCTAAGCAAA TGAATAGCTT AGAGGTGAAT ACTGAATCTT 180
TTGCTTCAAG TAGCTCAGCA TTTTTGTCTT TCATTTTTAC TAAGTGACTA GATTCAGTAT 240
TCGAAGATGT TTTGGCCAAA TGATTCATTA TTTATTTGGC TTTAGAAAGA GACTTCAAAA 300
GGATAATAGA AATAAACAAC CCAGAGGTTT TTTTTTTAAA TTGAAGATTA ATAAAAGAGA 360
GACCTCTGCT GGCTACAGTG GGGTAACAAC CTAGAGTTGG CCACTGACTC CACAGGAAGC 420
TATAATGGCT GTGACCCACC CCATACGCTT TTACAGTTGT CAGCAAATTG ATCACTATTT 480
GTTCACTTCT TCAGCAATCA ACTCAAGTTC TTTTGGAGTT CATTGAAGTG AGGTATAATT 540
CCCAGTCCAA TCACCACTGT TTCTGTTTCA ATCTTTAGGA AAAGTATTAG TCTTTTATAT 600
TTCTCGAACA TAATAGCTTT ACATATGAGC CCCTGCCAAA CTGAGACCTG AAATAATTCC 660
TGCATCTTAC CTTCTCTGTT TCCTTTCCCC TTTTTTGCCT CCACCTCTCC TCCTCCCCTT 720
CTCCAGTAAA ACAAAATAAA ACAAATCTAC ACTCAAGAGA GAGTACTGAT AGAAAGTGAG 780
AAGGAGGGAG CTGGGCGCTT ATCTTTGGCA TATCCTCAGC TGAGGATCCA AGCTGGGGGG 840
CCCAGGGTTG GTGTTAACTA CCTGAGTAGA GCTGTAGTTC CTACTGATGT CTTCCGTGGG 900
ATTTGTTCAA CCGTGGGAAT GTGGCTGCAC GATAGTGGAG CAAGATTCAG TGAATGCTTC 960
AGAATATGGA GGGTCGTTAT CTAGGGGGAG GAAGGGGACT GAATGTTCTC TTGAGACCTT 1020
TTGTTGGCAA CAACAATAAT GAGTGCCTAC TATGTGCCAG GCCCTGGACT AAGTACCTTA 1080
AATACCTTAA TTCTGTTTCC TGCTTTTCTT CTCTCTTCAC AGTCTTAAGA ATGTCTTTCT 1140
ATGAGAAAAA CATTGAATAT ATGTAAAGAA CTTACAACAA GGCCTGCATA AAGTAGTAGC 1200
TATGCATGTG TTCACTATTT TATTATTATG TTTTTACTCT GGAATATGCT GCCACTCCTA 1260
CACATGAGGA GAGGCTCTCC CCATACTCAC CAGAGCAAGC AAGTCCTTTT TTTTTTTTTT 1320
TTTTTTAAGA CACATGGAGT CTTGCTCTAT TGCCCAGGCT GCAGTGCAGT GGCATGATCA 1380
TGGCTCACTG CAGCCTCGAC CTCTTGGGCT CAGGCAGTCC TCCTGCCTCA GCCTCCTGAG 1440
TAGCTGGGAC TGCAGGTGTA TGCCACCACA CCTGGCTAAT TTTAAATTTT TTAGAGATGG 1500
GGTCTCACTA TGTTGCCCTG GCTGGTCTTG AACTCCTTTG CTCAAGCAGT CCTCCCAACT 1560
TAGCCTCCCA AATCATTGGG ATGAGAAGCA TGAACCACTG TGCCTGGTTA ATTACATAGA 1620
TATTTACATA TCTACTATCT TAAAACGGTG TCCTTTTAAG AATTTCAAAT GATGCTTTAT 1680
AGTTTCTAAT ATGGTGCACT GGGTATACTG TTGATATTTA AAGTTTTGTG AATGATAAAT 1740
TTCCCTACTT CAGTAGTGCC ATAGAATTAA TTGATTCTTG TATCTGAAAT TTAATGAGTG 1800
CTTATGAAGT ATGCTGGACT GTGCTAGGTT CTGACAGCAT TTGAAAAGAA GTTTGACATC 1860
TGCCTGTCTG TCCCCTTTTG GCTGCCTATG AGGTGTGTAA GATGGCTGCA ATTTGAGGAG 1920
GCATCCTTTG TTCCTGAGGA TAGAAGGTGC ATTGTGGAGT AGAAAGATAC AGGAACTATA 1980
GGCGATGCCA CACCAACTCT GTGCCACTTA TCTCCAGAAT TCCTGTACAG AAAAGAAAAG 2040
TACACTTTTA 2050