EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS017-00941 
Organism
Homo sapiens 
Tissue/cell
CD14+_monocyte 
Coordinate
chr1:43408990-43411490 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs12718444chr143409179hg19
TF binding sites/motifs
Number: 7             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
IRF1MA0050.2chr1:43411042-43411063AAAACAAAAGCGAAACCAAAA-7.53
IRF2MA0051.1chr1:43411046-43411064CAAAAGCGAAACCAAAAA+7.35
IRF9MA0653.1chr1:43411044-43411059AACAAAAGCGAAACC+6.33
SPI1MA0080.4chr1:43410014-43410028AAAATGAGGAAGTC+6.32
SPICMA0687.1chr1:43410349-43410363CGAAAGAGGAAGAA+6.08
SPICMA0687.1chr1:43410014-43410028AAAATGAGGAAGTC+6.68
SREBF2MA0596.1chr1:43410992-43411002ATCACCCCAT-6.02
Number of super-enhancer constituents: 48             
IDCoordinateTissue/cell
SE_01795chr1:43403674-43411142Aorta
SE_02447chr1:43405569-43410613Astrocytes
SE_05390chr1:43406422-43410832Brain_Cingulate_Gyrus
SE_06192chr1:43406287-43411226Brain_Hippocampus_Middle
SE_07319chr1:43406534-43411143Brain_Hippocampus_Middle_150
SE_08269chr1:43406272-43411134Brain_Inferior_Temporal_Lobe
SE_10377chr1:43406726-43412417CD19_Primary
SE_11009chr1:43387831-43425728CD20
SE_12470chr1:43408918-43409642CD3
SE_13825chr1:43408814-43412632CD34_Primary_RO01536
SE_14471chr1:43395753-43414527CD4_Memory_Primary_7pool
SE_19657chr1:43406292-43410967CD4p_CD25-_Il17p_PMAstim_Th17
SE_20345chr1:43407577-43412424CD56
SE_20799chr1:43405756-43409955CD8_Memory_7pool
SE_20799chr1:43409957-43412980CD8_Memory_7pool
SE_22754chr1:43406075-43412634CD8_primiary
SE_23189chr1:43406366-43410995Colon_Crypt_1
SE_23904chr1:43407223-43410890Colon_Crypt_2
SE_25177chr1:43406652-43411022Colon_Crypt_3
SE_26580chr1:43395721-43413249Esophagus
SE_29267chr1:43400819-43410293Fetal_Intestine_Large
SE_31882chr1:43406451-43411068Gastric
SE_33837chr1:43401475-43412846HCC1954
SE_34353chr1:43395339-43412997HCT-116
SE_35049chr1:43400682-43411164HeLa
SE_36013chr1:43405529-43411011HMEC
SE_37191chr1:43404622-43414101HSMMtube
SE_38794chr1:43405440-43410875HUVEC
SE_39883chr1:43405665-43410931K562
SE_41038chr1:43405665-43414583Left_Ventricle
SE_41620chr1:43406373-43411014LNCaP
SE_42796chr1:43405575-43411121Lung
SE_42796chr1:43411152-43414315Lung
SE_49782chr1:43407568-43410944Right_Ventricle
SE_50202chr1:43406339-43411463Sigmoid_Colon
SE_54088chr1:43408884-43411067Spleen
SE_55340chr1:43407386-43410138Thymus
SE_55340chr1:43410345-43410828Thymus
SE_55821chr1:43405505-43410178u87
SE_57045chr1:43406294-43410932VACO_400
SE_57417chr1:43405825-43410963VACO_503
SE_58561chr1:43388242-43430420Ly1
SE_60624chr1:43388552-43428820DHL6
SE_62392chr1:43388423-43425814Tonsil
SE_64094chr1:43405747-43410036HSMM
SE_64340chr1:43405657-43411071NHEK
SE_67781chr1:43405505-43410178u87
SE_68708chr1:43406265-43410984H9
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 1             
ChromosomeStartEnd
chr14340968043410322
Number: 1             
IDChromosomeStartEnd
GH01I042929chr14339554143414526
Enhancer Sequence
TTCTGCGGAG AAACAAACCA CACTGTTATA GGCGTGTCTG GGAGCAGGTT ACTACAGGGC 60
AGGGCCTGGA CTGGCAAGTT TCTGTGTTCA GATATCTTGC CTGACTCTTG GCACCACACC 120
AGTCTTTCTC CCAGGAAACT TGGCCAATTC CTGACCTTAG GTGCCCAAAC CAGCCTAGCT 180
GACTTCAAGA TACTGGGCTG GCCGGGCCAT TTCCTGGGGA GAGAGGGGAA GTATGATCTT 240
CTCTCTCTGT AGCCAGGTCT CAGAGAGGGA GAGGCTTTGG ATTCTTGGGG GTCTCATTTC 300
CCTGGTGGAG CCATGCCTAG GGTCTGGTGG TTCTAGACTC TCTGACTGGG AGGCCCAGGA 360
ACCAGCCCTC CTATGCGAGG GGGCCCAAAT TACTTGGTAG GAATAGCACA GATATAGATA 420
GGAGAAGCAC CCTGGATTTG GAGCTGAAGC CGCTGGCTTC TGATTCCAGC CCATCTGCCT 480
GTTTGCTCTG TGAATTCCAG CAGGCTAAGT CCCCCATGTA CCACCTCTCC CCTATCCTCC 540
ATTTGCTTGT CAGCAAAATG GCAACAGCTT CGTTTGTCAC ATTGGAGATG TGATCCCACC 600
TTGCCCTACC CTTCCTGCTG TTCACAGGGC AGGAAACTGA GCCCTGAGAG GGTGAGGCAA 660
GTTCCAGATC ACTCAGGAGC CTGCAGCAGA GCTCAGGGCT CCGGACTCCT TACCCAGTGC 720
TCCTCACGGC AATAATCCCC AAACCATAAG CCTCCCAAGG TTATATGGAC ATAGACGACA 780
TGCTAGGCGG GAATGCACTT TGGAAAAGTG CACAAGGTGA GTAAGAGTGT GGGGCTAAGG 840
TGTTTCCAAT GGGCAAAGGG ATGGGAGAGA AAAAGAGCAG TTTGCTTCTG TCCATTGGAA 900
GCCGAGGACC TAAGGCAGCA GGAAGGGCAG AGGCCAGCAG GTGAAGAGCC CTGCTTAGCC 960
ACAGGTGACT GAGAGGCCAG CAGGGTGTCA GCCCTGCTGA AGAAAAGTGC TCTTTTCAGC 1020
TATAAAAATG AGGAAGTCAG GAAATGTGAC ATTAGGCAGG CCTTTAACTG ATTGTGGGAG 1080
AACAGGGCTG CGGGAGGCAT GCCAAAGAAA CGACTGGCAT TCACTACGCA CACTATACCA 1140
AGCTGGGCCC TGGAAGTGGG TGGAGCTGGC CATGGCCTGG CTGTGGGTCT CTGGGCCTTG 1200
GTTTCCACAG AACCCAGAAG CAGCCTTTAC TTCAAGATCA TCACAGATAG CCCTGGGCAT 1260
AGCTGTTACC AGGCATATTC CCAGTATGGT CTTTTCATTC TCTGAAAGCG TCAGTCAGGG 1320
CAACGACTGC AAAAGCCAAG GCTCTCACAT CAGAGGCTGC GAAAGAGGAA GAAGGCTTCG 1380
GCCCAGGAGG AGTGTGCAGC TCAGAGCCCC CTCTGTGTGT GCGCTGCATC CTTCCTTCCC 1440
ATTAGTCTGT CTACCTGACC CCTTAGCCTG CCTCTGGACA TTTATTCCAC ATGCTGGGGC 1500
TTCCCTCATA CCACAGGGAC TCCATTCCCT CTAAATCCTC TGCATTGCCC AACTAGAAAG 1560
ACAGCCCCCA CCCCCCGTAT GTCCTGGCAC TGCCCCCAGA ATCTCCCTTC TCTCAATTCT 1620
CTGGGGAGCC TTCAGGCCCA GAGCTGTTGT TCCGAGTGGG TAGTGAGCAG CTGACAAATT 1680
TCTGGGGGAC CCCAGCGACA CACCAGGTCA AGCCTAATTC ATAGGGTGGA CACTAATTCA 1740
GAGGCTGTGG CAAGGCACTA AGCATCACCA GGAGGGCTCA CTAAACAGCG ACTGCTAGGC 1800
CCGCCACGTG CTGGGCTTTC TGCCTGCGGT ATTACCTGCA TTTGCTCATG GGATGCAAAG 1860
TATATACTGT ATTTTTCTGG AACACATTAG AATAGATTAA AAAACAAGCA ATGCAGTGAC 1920
ATCAATCTAT CATTTAAGAA AACGTGGCAT AGTGATATAA TGGAATACAT AACCTGGGAG 1980
TTCGAGGCCG CAGTGAGCTG TGATCACCCC ATGGCACTCC AGCCTGGGTG ACAGAGTGAG 2040
ACTCTGTCCC AAAAAACAAA AGCGAAACCA AAAACAGAGC AGTGTGTATA TTGTATGCTA 2100
CCTTTTGGGT TAAAAAAAAA AATTGGCTGG GGGTAGGGGG AGAATATACA CATCTATTTA 2160
AAAGAATGCA CAAGAGGCTA GGCACGGTGG CTCACATCTA TAATCTCAGC TTGAGGCCAG 2220
GAGTTCGAGA CCAGCCTGGC CAACATGGCA AAACCCTGTC TCTACTAAAA ATACAAAAAT 2280
TAGCTGGGCA TGGTGGTGCG TGCCTGTAGT CCCAACTACT TGGGAGGCTG AGGGACAAGA 2340
ATCACTTTAT CTGGGAGATG AAGTGAGCCG AGATGGCGCC ACTGCACTCC AGCCTGGGCG 2400
ACAGAGCAGA CTCTGTCTCA AAAAAAAAAA AAAACAAAAA ACAAAAAACA AGAATGTACA 2460
AGAAAGGTAA CATTCTAACC CCGGGGGGGC CTGGGTGACT 2500