Variant report

Variant	rs11968400
Chromosome Location	chr6:31804729-31804730
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:153)
CpG islands
(count:0)
Chromatin interactive
region (count:22)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:153 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr6:31801322-31807327	K562	blood:	n/a	n/a
2	CTCF	chr6:31804600-31804750	AoAF	blood vessel:	n/a	n/a
3	CTCF	chr6:31804620-31804770	AG04449	skin:	n/a	n/a
4	CTCF	chr6:31804680-31804830	HCM	heart:	n/a	n/a
5	CTCF	chr6:31804511-31804855	K562	blood:	n/a	n/a
6	POLR2A	chr6:31804561-31805330	U87	brain:	n/a	n/a
7	EP300	chr6:31804522-31804898	K562	blood:	n/a	chr6:31804788-31804798
8	ZNF263	chr6:31804517-31805748	HEK293-T-REx	kidney:	n/a	chr6:31804723-31804732 chr6:31804638-31804647
9	SPI1	chr6:31804724-31805058	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:31804583-31805234	K562	blood:	n/a	n/a
11	CTCF	chr6:31804600-31804890	NHDF-neo	bronchial:	n/a	n/a
12	TBL1XR1	chr6:31804649-31805603	K562	blood:	n/a	n/a
13	CTCF	chr6:31804600-31804750	AG04450	lung:	n/a	n/a
14	CTCF	chr6:31804600-31804750	HA-sp	spinal cord:	n/a	n/a
15	POLR2A	chr6:31801892-31807499	GM12892	blood:	n/a	n/a
16	CTCF	chr6:31804660-31804810	AG04450	lung:	n/a	n/a
17	POLR2A	chr6:31801963-31810342	PANC-1	pancreas:	n/a	n/a
18	CTCF	chr6:31804620-31804770	HBMEC	blood vessel:	n/a	n/a
19	POLR2A	chr6:31804715-31804984	Hela-S3	cervix:	n/a	n/a
20	POLR2A	chr6:31804551-31805130	U87	brain:	n/a	n/a
21	IRF1	chr6:31803770-31805820	K562	blood:	n/a	chr6:31804381-31804395
22	POLR2A	chr6:31804574-31805878	HepG2	liver:	n/a	n/a
23	CTCF	chr6:31804580-31804730	AG04449	skin:	n/a	n/a
24	POLR2A	chr6:31803643-31807146	HL-60	blood:	n/a	n/a
25	POLR2A	chr6:31804720-31806381	GM12891	blood:	n/a	n/a
26	CTCF	chr6:31804600-31804750	RPTEC	kidney:	n/a	n/a
27	CHD1	chr6:31802371-31805289	H1-hESC	embryonic stem cell:	n/a	n/a
28	SPI1	chr6:31804662-31805164	HL-60	blood:	n/a	n/a
29	POLR2A	chr6:31804430-31805503	GM12891	blood:	n/a	n/a
30	POLR2A	chr6:31803729-31805859	K562	blood:	n/a	n/a
31	TEAD4	chr6:31803538-31805859	K562	blood:	n/a	n/a
32	CTCF	chr6:31804600-31804750	AG10803	skin:	n/a	n/a
33	HEY1	chr6:31801932-31809366	HepG2	liver:	n/a	chr6:31802428-31802443
34	MYC	chr6:31802073-31805549	K562	blood:	n/a	chr6:31802670-31802680
35	CTCF	chr6:31804600-31804750	SK-N-SH_RA	brain:	n/a	n/a
36	CTCF	chr6:31804660-31804810	GM12873	blood:	n/a	n/a
37	ZMIZ1	chr6:31804665-31805340	K562	blood:	n/a	n/a
38	POLR2A	chr6:31802091-31809648	K562	blood:	n/a	n/a
39	POLR2A	chr6:31801829-31816167	SK-N-MC	brain:	n/a	n/a
40	MAX	chr6:31801806-31804734	K562	blood:	n/a	chr6:31802670-31802680
41	CTCF	chr6:31804580-31804730	Caco-2	colon:	n/a	n/a
42	FOS	chr6:31804720-31805051	MCF10A-Er-Src	breast:	n/a	chr6:31804954-31804963
43	CTCF	chr6:31804620-31804770	GM12872	blood:	n/a	n/a
44	MAZ	chr6:31804453-31804817	K562	blood:	n/a	n/a
45	TBL1XR1	chr6:31804001-31805904	K562	blood:	n/a	n/a
46	POLR2A	chr6:31802046-31807267	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:31804600-31804750	BJ	skin:	n/a	n/a
48	POLR2A	chr6:31801886-31806082	GM12892	blood:	n/a	n/a
49	TEAD4	chr6:31804562-31805618	HepG2	liver:	n/a	n/a
50	POLR2A	chr6:31802009-31806310	HUVEC	blood vessel:	n/a	n/a

No data

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:31800755..31815108-chr6:31823340..31833266,54	K562	blood:
2	chr6:31800806..31810142-chr6:31827604..31833040,24	MCF-7	breast:
3	chr6:31702549..31706090-chr6:31802474..31805993,4	MCF-7	breast:
4	chr6:31509889..31512472-chr6:31802635..31805585,2	MCF-7	breast:
5	chr6:31737226..31750413-chr6:31786206..31805473,50	MCF-7	breast:
6	chr6:31801616..31806746-chr6:31865132..31870777,8	MCF-7	breast:
7	chr6:31508602..31511012-chr6:31803135..31806104,3	K562	blood:
8	chr6:31802844..31805158-chr6:31938598..31941453,3	K562	blood:
9	chr6:31803796..31805306-chr6:32094285..32096124,2	K562	blood:
10	chr6:31798354..31804916-chr6:31860790..31871982,18	MCF-7	breast:
11	chr6:31802366..31805115-chr6:31938170..31940148,2	K562	blood:
12	chr1:181056898..181058839-chr6:31802790..31804747,2	MCF-7	breast:
13	chr6:31696408..31700150-chr6:31800226..31805691,5	MCF-7	breast:
14	chr6:31630921..31635353-chr6:31802314..31807064,6	MCF-7	breast:
15	chr6:31735011..31745595-chr6:31798203..31806127,22	MCF-7	breast:
16	chr6:31801090..31813654-chr6:31824519..31834411,41	MCF-7	breast:
17	chr6:31800867..31807275-chr6:31862460..31868132,16	K562	blood:
18	chr6:31802757..31805057-chr6:31913533..31915744,2	MCF-7	breast:
19	chr6:31800669..31805219-chr6:31862460..31868046,11	K562	blood:
20	chr6:31802718..31804825-chr6:31935287..31937664,2	K562	blood:
21	chr6:31800580..31812447-chr6:31823435..31837480,47	K562	blood:
22	chr6:31697326..31699677-chr6:31802341..31805046,2	MCF-7	breast:

No data

Variant related genes	Relation type
SNORD52	TF binding region
ENSG00000204385	Chromatin interaction
ENSG00000213722	Chromatin interaction
ENSG00000204386	Chromatin interaction
ENSG00000204396	Chromatin interaction
ENSG00000213676	Chromatin interaction
ENSG00000213719	Chromatin interaction
ENSG00000204348	Chromatin interaction
ENSG00000204351	Chromatin interaction
ENSG00000204435	Chromatin interaction
ENSG00000162783	Chromatin interaction
ENSG00000204366	Chromatin interaction
ENSG00000198563	Chromatin interaction
ENSG00000204371	Chromatin interaction
ENSG00000234006	Chromatin interaction
ENSG00000204438	Chromatin interaction
ENSG00000243649	Chromatin interaction
ENSG00000201207	Chromatin interaction
ENSG00000166278	Chromatin interaction
ENSG00000265236	Chromatin interaction
ENSG00000263020	Chromatin interaction
ENSG00000204344	Chromatin interaction
ENSG00000201555	Chromatin interaction
ENSG00000204394	Chromatin interaction

Extended variants
information (count: 33 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs12193504	0.94[ASN][1000 genomes]
rs12210887	0.90[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs12212242	0.94[ASN][1000 genomes]
rs13191375	0.94[ASN][1000 genomes]
rs2075799	0.82[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs3869144	0.90[ASN][1000 genomes]
rs693906	0.90[ASN][1000 genomes]
rs73400280	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7765136	0.94[ASN][1000 genomes]
rs9461726	0.82[AFR][1000 genomes];0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:23 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv601610	chr6:31280101-31960770	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	370 gene(s)	inside rSNPs	diseases
2	nsv601628	chr6:31280327-31990098	Weak transcription Transcr. at gene 5' and 3' Active TSS Enhancers Flanking Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
3	nsv601629	chr6:31280327-31996185	Strong transcription Enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	376 gene(s)	inside rSNPs	diseases
4	nsv601630	chr6:31280327-32011317	Genic enhancers Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
5	nsv601631	chr6:31280327-32017540	Genic enhancers Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	378 gene(s)	inside rSNPs	diseases
6	nsv1023939	chr6:31325961-32026747	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
7	nsv538188	chr6:31325961-32026747	Active TSS Weak transcription Flanking Active TSS Enhancers Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	372 gene(s)	inside rSNPs	diseases
8	nsv1021747	chr6:31386219-31907266	Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Enhancers Genic enhancers Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	330 gene(s)	inside rSNPs	diseases
9	nsv1033154	chr6:31550614-32009410	Strong transcription Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	326 gene(s)	inside rSNPs	diseases
10	nsv1017945	chr6:31609641-32481240	Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	322 gene(s)	inside rSNPs	diseases
11	esv3428142	chr6:31615800-31881809	Flanking Active TSS Active TSS Weak transcription Enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	257 gene(s)	inside rSNPs	diseases
12	nsv884428	chr6:31728102-31870326	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	162 gene(s)	inside rSNPs	diseases
13	nsv884429	chr6:31730356-31837066	Enhancers Transcr. at gene 5' and 3' Strong transcription Active TSS Weak transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	155 gene(s)	inside rSNPs	diseases
14	nsv462872	chr6:31778272-31864304	Enhancers Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
15	nsv601945	chr6:31778272-31864304	Flanking Active TSS Strong transcription Weak transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	144 gene(s)	inside rSNPs	diseases
16	nsv601950	chr6:31785438-32492308	Enhancers Bivalent Enhancer Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
17	nsv601951	chr6:31785438-32496748	Enhancers Flanking Active TSS Strong transcription Weak transcription Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
18	nsv884461	chr6:31785453-31827045	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	117 gene(s)	inside rSNPs	diseases
19	nsv601955	chr6:31785453-32484368	Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	196 gene(s)	inside rSNPs	diseases
20	nsv601956	chr6:31785453-32492308	Strong transcription Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	197 gene(s)	inside rSNPs	diseases
21	nsv462874	chr6:31794592-31864304	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
22	nsv601959	chr6:31794592-31864304	Strong transcription Enhancers Weak transcription Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	118 gene(s)	inside rSNPs	diseases
23	nsv884463	chr6:31797422-31827045	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31801400-31805000	Active TSS	Pancreatic Islets	Pancreatic Islet
2	chr6:31801600-31805000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr6:31801800-31805000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:31802000-31807000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr6:31802200-31804800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr6:31802200-31806400	Transcr. at gene 5' and 3'	Primary T helper 17 cells PMA-I stimulated	--
7	chr6:31802600-31806400	Transcr. at gene 5' and 3'	HUES6 Cell Line	embryonic stem cell
8	chr6:31802800-31805000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
9	chr6:31802800-31806400	Transcr. at gene 5' and 3'	iPS-15b Cell Line	embryonic stem cell
10	chr6:31802800-31807400	Transcr. at gene 5' and 3'	iPS-20b Cell Line	embryonic stem cell
11	chr6:31803000-31805000	Flanking Active TSS	Primary B cells from cord blood	blood
12	chr6:31803000-31807400	Transcr. at gene 5' and 3'	K562	blood
13	chr6:31803000-31817200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr6:31803200-31805400	Flanking Active TSS	Primary hematopoietic stem cells	blood
15	chr6:31803400-31804800	Weak transcription	Spleen	Spleen
16	chr6:31803400-31805400	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
17	chr6:31803400-31806400	Transcr. at gene 5' and 3'	H1 Cell Line	embryonic stem cell
18	chr6:31803600-31804800	Flanking Active TSS	Fetal Adrenal Gland	Adrenal Gland
19	chr6:31803600-31804800	Flanking Active TSS	Fetal Brain Female	brain
20	chr6:31803600-31804800	Flanking Active TSS	Fetal Heart	heart
21	chr6:31803600-31805000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr6:31803600-31805400	Transcr. at gene 5' and 3'	ES-I3 Cell Line	embryonic stem cell
23	chr6:31803600-31805400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
24	chr6:31803600-31805400	Flanking Active TSS	Brain Germinal Matrix	brain
25	chr6:31803600-31806200	Transcr. at gene 5' and 3'	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr6:31803600-31807000	Transcr. at gene 5' and 3'	HUES64 Cell Line	embryonic stem cell
27	chr6:31803800-31804800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
28	chr6:31803800-31804800	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
29	chr6:31803800-31804800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
30	chr6:31803800-31804800	Flanking Active TSS	Brain Hippocampus Middle	brain
31	chr6:31803800-31804800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
32	chr6:31803800-31805000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
33	chr6:31803800-31805000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
34	chr6:31803800-31805000	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
35	chr6:31803800-31805000	Flanking Active TSS	Brain Anterior Caudate	brain
36	chr6:31803800-31805200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
37	chr6:31803800-31805200	Transcr. at gene 5' and 3'	Fetal Stomach	stomach
38	chr6:31803800-31805400	Transcr. at gene 5' and 3'	Left Ventricle	heart
39	chr6:31803800-31805600	Transcr. at gene 5' and 3'	Fetal Muscle Trunk	muscle
40	chr6:31803800-31805800	Transcr. at gene 5' and 3'	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:31803800-31805800	Transcr. at gene 5' and 3'	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr6:31803800-31805800	Transcr. at gene 5' and 3'	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:31803800-31805800	Transcr. at gene 5' and 3'	Fetal Intestine Large	intestine
44	chr6:31803800-31805800	Transcr. at gene 5' and 3'	Fetal Intestine Small	intestine
45	chr6:31803800-31805800	Transcr. at gene 5' and 3'	NHEK	skin
46	chr6:31803800-31806000	Transcr. at gene 5' and 3'	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr6:31803800-31806000	Transcr. at gene 5' and 3'	ES-UCSF4 Cell Line	embryonic stem cell
48	chr6:31803800-31806400	Transcr. at gene 5' and 3'	H9 Cell Line	embryonic stem cell
49	chr6:31803800-31806400	Transcr. at gene 5' and 3'	Dnd41	blood
50	chr6:31803800-31806400	Transcr. at gene 5' and 3'	Osteobl	bone

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