EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS098-11063 
Organism
Homo sapiens 
Tissue/cell
HSMM 
Coordinate
chr11:95990180-95993010 
SNPs
Number: 1             
IDChromosomePositionGenome Version
rs11021499chr1195992129hg19
TF binding sites/motifs
Number: 11             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
CDX2MA0465.1chr11:95991149-95991160TTTTATGGCCT-6.02
Foxd3MA0041.1chr11:95991514-95991526AAATGTTTGTTT+6.27
Gfi1bMA0483.1chr11:95990419-95990430AAATCACAGCT+6.14
Gfi1bMA0483.1chr11:95991686-95991697AGCTGTGATTT-6.14
IRF1MA0050.2chr11:95991347-95991368TTACTGAAAGTGAAACTTATA-6.64
IRF1MA0050.2chr11:95991563-95991584AGAATGAAACTGAAAGAGGCA-6.76
IRF2MA0051.1chr11:95991351-95991369TGAAAGTGAAACTTATAA+6.4
IRF8MA0652.1chr11:95991350-95991364CTGAAAGTGAAACT+6.19
Lhx3MA0135.1chr11:95991185-95991198AATAAATTAATTT-6
TBPMA0108.2chr11:95992060-95992075CCCAGCCTTTTATAC-6.22
ZBTB18MA0698.1chr11:95992404-95992417TTTCCAGATGTTT+6.28
Number of super-enhancer constituents: 26             
IDCoordinateTissue/cell
SE_00421chr11:95990695-95994185Adipose_Nuclei
SE_09528chr11:95988993-95993093CD14
SE_10685chr11:95986205-95993908CD19_Primary
SE_11167chr11:95985208-95994550CD20
SE_12380chr11:95989202-95994108CD3
SE_15173chr11:95986487-95994286CD4_Memory_Primary_7pool
SE_16197chr11:95988978-95990594CD4_Naive_Primary_7pool
SE_16197chr11:95990631-95994008CD4_Naive_Primary_7pool
SE_17498chr11:95985112-95995021CD4p_CD25-_CD45RAp_Naive
SE_18301chr11:95989089-95994399CD4p_CD25-_Il17-_PMAstim_Th
SE_30644chr11:95990730-95992362Fetal_Muscle
SE_31211chr11:95989224-95993674Fetal_Thymus
SE_36675chr11:95990838-95992393HMEC
SE_36675chr11:95992462-95993458HMEC
SE_44431chr11:95990759-95993077NHDF-Ad
SE_45599chr11:95989581-95994498Osteoblasts
SE_50559chr11:95989228-95991195Sigmoid_Colon
SE_50559chr11:95991362-95993946Sigmoid_Colon
SE_53120chr11:95990321-95991278Small_Intestine
SE_53120chr11:95991353-95993089Small_Intestine
SE_54051chr11:95989201-95991313Spleen
SE_54051chr11:95991340-95993046Spleen
SE_58447chr11:95917840-96001635Ly1
SE_61108chr11:95917662-96027831HBL1
SE_61760chr11:95940172-96001818Toledo
SE_62369chr11:95920962-96006907Tonsil
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 2             
ChromosomeStartEnd
chr119599030895990455
chr119599144295991675
Number: 1             
IDChromosomeStartEnd
GH11I096253chr119598625295993991
Enhancer Sequence
ACAGGGATTA CCTTGTAAAA ATACAGTTTC CAGCAGACCA AAAATAGGCA CAATGTTTCT 60
GTGATCCCAA CTTTTGCATT CAGCATTTTG AGAGGTTTTT CTGTGGAAAA GCATTTCCAA 120
TTTTACAGTA GAGTTGTAGA CAAATGTTGC AATTTATTTA AGCTTTGTTT TATTGTCAAA 180
TTTCCTGTAG CCCATCCACT CCATGAAGCA AGAGATAACT GGTTTGCATC ATCTTTTTAA 240
AATCACAGCT CTGGATCTGC ACTATTGGAA CACTCTCTTG TCACCCTGCA ATTGATCCTT 300
TCATACTTCT TTCTCCTCCA TTGGACTGTA AGTTCTTGAA AGTGGGAATC TTGTGACTCC 360
AATTTTTCAA TACTGAGCAC AGTGCTGGCA CAGAATATGA ACTCACTATA TCTTGTTACT 420
ATAAATGAAT AAACAAAATG CATAGGCATG TTAGGCATTT AGTAAATACA TGTCAAATTG 480
AATCTTTGAT ACATGACTTG GAATTACTTC CCTTTCAAGG TATTTGTTCA GTGAGCATAA 540
TTATAGAGTC CACAGTCTAA CAGTCTTCAT TATAGAGAAA AACCGAAAAA GAGCCCTTGG 600
CTTTTCAAGA CAATATGCAT TGATGGCAAC CCCCTTTTTA TCATGTGCAT ATTTCATGCA 660
CAAGGACAAC TTAAAACTTG GAATGAAAAA AAAACCTCTA TAATATTTCT TTGCTCACCA 720
GTGCTGCCCA TTTCTGGTAT TCTCTCTTTA CTGTGTATCC TGGGGGTGAT GGGAAGAAGA 780
GGAGAGACGA GAAGGACTTA CTAGTAACAG AAAGGAAAAT AATGAATTGG GAAGAGGAGC 840
AAAGGGGATG GTGAGGACTG GAATAACAAC TTTATAAAGA ATAAAAGTCT GATTCCCTTC 900
TATTTCCTGC AGTCTCTCAT TGCTCCTGTC TCTGATAAAA TGCCTACAGA TTTGCTTACT 960
TGATCCTAAT TTTATGGCCT GTTCAAATAT TACAACTTCT TTTTAAATAA ATTAATTTGG 1020
AACTAAATGC CTTTAATTTT TACCGTGATA GGTTTGTGGC TCTTGACATC TTTTGGTCCT 1080
ATTCATCAAA ATCATTTGCT AAGTCCAAGG TATAGCAGAG TGGCTTTAAC AACAACCATG 1140
GAGGATGAAT AAAATACATT TTCATATTTA CTGAAAGTGA AACTTATAAG CATATATCAT 1200
CTTCTGCCTA CCTTGTAAAT ATCCCATGTT TTCATTTACA TATTGTACCA ATTAATATAT 1260
CTTGGTACTA ATCAGAGTGG AATCCACTCC TGACATGGGA GAAAACTACG ACAAAAAACA 1320
TTAGCAGCAA GAAAAAATGT TTGTTTCAAG TATGTGGATT ATATTTTCTA GTGCCTTAAA 1380
AAAAGAATGA AACTGAAAGA GGCAGCTTGA AGAAGCTTAC ATGTGTTTAA AACCCACATC 1440
CTGTTGTTAT CCACTGCCCT GGCACAGAGG AGCTGGGAGG TGAACGTCCT CATTAGGGTC 1500
CCTATTAGCT GTGATTTGCA ATGGGCTTCT CCAAAGAAGA AAATCACATT CACCCACTGG 1560
ACAATGGCCC AGGTATCACC ATTGATGGGA ATCATATATG GAGTAAACAT CAAAGCCCAA 1620
GAATACAGTG GTCTAAGCCA GTGTGCTTAG AAGTTGCCAG ATCCTCCATG CTTCATTCCA 1680
GCCACTATCA GCAGATTCTA AATCACCTAT GAGCAGAGAG GCCCATCTGC CTAGGGCATA 1740
AACGAAATTA TAACAACAGT GAGAGAGCCA ATGGGAGTCA GCCAGTAAGA CTATGAGCAG 1800
CATGATGTAC TCAGACTTTT GTTCCTTTTT ATTTATTTGG TTAAAATACA TGTGTTTTTG 1860
CTTCAGGCAG ATGTTGGTAT CCCAGCCTTT TATACAGGAA GCTGTAGAAG GGAGAGGACT 1920
TTCTGGGTGG GAGCAACTTA TTGTGGAGGC CAAATGGCAT TTTTTGTAGG CCCTGAGATT 1980
TTTTACGAAA ACACTAACTC TGTTCAGAAC TCTTTCAAAG GGTGAAGACA AACTTAACAA 2040
CCTTATACTA TAATACAAAT AATTACAGAG TGTTGCTTTA AACTTGTATC TTGAAGTTCC 2100
TTCTTTAGGT AACTCTGCTT AACAACCACA GACTCTTCTT CCTAATGGCT TATCTGCATG 2160
TCTTTTCAAT TTTCTAAGTG AAGGCCAGCC CCCTTCAAGA TGTTCTACCA ACTCAGTCCT 2220
ATTCTTTCCA GATGTTTTTT TTCTTTTTCT TCTTCTGAAA AGCATGTGTT GATAGACTAT 2280
GGGGAACAGA CCAAGATTTA TTTTTTAGCC AGCATTTTCC CCTTGCAACC GTAAGTCATT 2340
CTTCCTCAGA AGGCAAGGTG GGGCAAGTGA TTCTAATGTG CTTCGCTCCA ATGCTTCCAT 2400
CTCAATAACC CTTTAAAGTG AAAACTGTGG AGAGTGAAGT GAAAAACTTG TCTCCATCTG 2460
GAAGCATTTA TACAGAGAGG TGTCTTTAGC TTAGTTGTTT GTCTAGAATT TCCATTTATG 2520
AACCGACTTG CCTTTCTCCT GTGGGTATGC TGGAGAAAAC TCTTTGCAAA ATCCATTGTA 2580
TGCAATAATC CAGTGGCTCC TTCAAACTCA ATCAGGCTGG AAAGGCTAAA TATGACTCAT 2640
AGGATTCCTC CAACAAACAC AAAGTAAGTC AGAAGTCAAG GAGAGAGTCA TCTCGATGTG 2700
GACCAGCTTA CCTAGCAAGG CAGGGAATTG TCATAAAACC AGTTTCCTGC TTGCAAGACC 2760
TTGACTCCTT TCAGTAAAGG TGTCAACTCT TCTTTTTCTG AACAATCTCA ATGTGAATGA 2820
CAGGGCCTGA 2830